Wednesday, September 21, 2022

Notes From Coffee With MGI

A couple of weeks ago  I sat down for coffee with a pair of MGI representatives - American Region CEO Yongwei Zhang and Director, Global Business Development Damon Zhang. Since I hadn’t been at AGBT 2022 (my 2023 application already filed!). Yongwei and I had planned to try to catch up the next time he was in Boston area, so I braved our current subway issues (not one, but two major lines shut for extended maintenance!) and covered a range of topics.

Tuesday, August 23, 2022

SRA Entries Should Not Ever Disappear Into Thin Air

I ran into an annoying problem last night and was quite steamed, but had the discipline to wait until morning to vent publicly about it.  Now I'm more in a morose mood on the subject, not furious but still quite frustrated. The quick version of what happened is I'm belatedly trying to go through some nicely documented reproducible analysis code to explore some concerns I have with the analysis, and the code is working on an SRA entry -- and that SRA entry is the entire point of the analysis. And that SRA entry which I know once existed now doesn't - other than this code and the preprint to go with it, it's as though it never existed -- which is terrible.  And I'm irritated with everyone who contributed to that terrible result, starting with NCBI

Tuesday, August 16, 2022

Supply Stall Slows Singular

Singular Genomics reported earnings last week and delivered an unpleasant surprise: inability of suppliers to make timely deliveries of key (but unspecified) hardware components have slowed G4 instrument production to a very slow crawl.  Given the lively competition in the desktop short read space, this is a serious setback for Singular's commercial launch.  

Thursday, June 23, 2022

AGBT 2022: Overhanging Questions

AGBT broke up a couple of weeks ago and I've failed to write anything here so far.  It was frustrating not attending, but not registering for a meeting in February seemed prudent given the pattern of COVID waves - I hadn't considered (nor would have wanted to bank on) AGBT organizers reacting so well and rescheduling the meeting.  It sounds like a number of attendees did catch the virus at the meeting -- though I'm presumably still quite protected by my infection a month earlier.  Anyways, I'm going to organize this around one to two questions that hover in my head for the different sequencing providers.  AGBT also had a strong spatial angle, but I feel ill-equipped to cover that in the absence of being on the scene -- I don't work with spatial data and so don't have a deep feel for it.  As always, please flag me here or on Twitter or by email for any errors I made -- or any juicy sequencing company gossip you wish to share!

Wednesday, June 08, 2022

Admin: Feedburner to Follow.it Switch

A bit over a year ago Google made one of their dreaded announcements that they would be slowly killing off one of their acquisitions, in this case FeedBurner.  Well over a thousand of you have been using FeedBurner to follow me via email.  Follow.it has a wonderful free plan that can take over all of the previous functionality and I could just import the old subscription list

Tuesday, May 31, 2022

Ultima Genomics Storms Out Of Stealth Promising $1/Gigabase Short Reads

To date, the new entrants targeting Illumina’s short read business have been aiming at the middle of Illumina’s range, trying to take on NextSeq.  Element Biosciences is touting high accuracy for a low price.  Omniome (now PacBio) also has positioned itself to tout accuracy.  Singular Genomics is claiming to enable great flexibility and fast runs.  But all aimed at NextSeq.  As part of the run up to AGBT another company is decloaking from stealth mode: Ultima Genomics, however they are going not after NextSeq but full throttle after Illumina’s pinnacle, the NovaSeq running the S4 flowcell.  The value proposition is a large sequencing device that delivers S4 output at S1 prices for an overall cost of $1 per gigabase.  Note that the interview for this piece was conducted under a CDA and Ultima reviewed my copy for accuracy and to ensure I didn’t disclose anything they had marked confidential.  They were nice enough to offer to have me fly out to their facility, but I was forced by the damn coronavirus to cancel those plans the night before the trip. A preprint summarizing the technology is also out in bioRxiv.  A trio of additional preprints have popped up as well, describing its application to generate a huge methylation sequencing dataset around colorectal adenocarcinoma, a huge Perturb-Seq dataset and for large scale single cell RNA-Seq.


Ultima isn’t planning on truly launching until early next year, but they’re well on the way with paying early access customers.  Indeed, AGBT will feature multiple posters and talks describing the use of the Ultima instrument for a variety of genomics tasks.  And Ultima is confident that their architecture will support significant increases in future throughput, enabling per base costs to go even lower.


Ultima’s chemistry is flow based - using unterminated but fluorescently labeled nucleotides.  Only a fraction of the nucleotides are labeled in each reaction, reducing the reagent costs and minimizing molecular scar accumulation.  The reactions take place on beads whose templates are amplified via emulsion PCR - though for all the ePCR-haters out there Ultima will include a fully automated benchtop ePCR robot.  Once primed, the beads retain the DNA polymerase, so this expensive component can be conserved between flows.  The instrument is a single end reader – no paired ends – but substitutes for that by reads with a modal read length of around 300 bases, which should be enough to plow all the way across most short read inserts and their associated molecular indices.


The use of unterminated nucleotides has typically meant challenges in resolving homopolymers.  Ultima is tuning their system to call homopolymers of up to 12 bases; via discussions with customers and their own experience accurate counting of longer homopolymers is deemed insufficiently valuable to focus on vs. other design tradeoffs.  


But Ultima has found several ways in which unterminated flow chemistry can either have its weaknesses ameliorated or become downright boons.  First, while it can’t accurately measure long homopolymers it can go straight through very long ones in a single extension cycle – so poly-A tails in cDNA ends can be easily blitzed through.  This helps ensure reading all the way through inserts of things like single cell libraries.  Second, for short homopolymers Ultima embeds in the Q-scores a probability matrix of the length – basically the odds of minus one and plus one versions of the sequence.  This is leveraged by their customized version of GATK, developed with the Broad Institute.  Third, is a clever approach of “cycle shift variant calling” that I’m still stunned has never appeared in the literature for any other flow chemistry – 454, Ion Torrent or Genapsys.  Cycle shift uses the known order of flows to increase the confidence in variant calls – particularly variable for low coverage data such as cell-free DNA.  


Another key driver of low cost and high density is the use of a spinning, open “flow cell” (really a 200mm diameter wafer) for both reagent addition and imaging.  Centrifugal force generated by the spinning (fake force, ha!) distributes the reagents as a very thin film, minimizing wastage.  Imaging as the wafer spins enables shooting many tiles without having to repeatedly accelerate and decelerate the flowcell as a rectilinear scanning scheme must do.  The speed difference adds up: Ultima can generate in 20 hours the same 3 terabases (10 billion reads of roughly 300 bases each)  as a NovaSeq S4, but an S4 requires 44 hours to run – and Ultima believes they can shave that down to 16 hours.  Faster cycle times means more runs per instrument – and each instrument runs two wafers simultaneously, each with its own chemistry station but sharing imaging path  The instrument features tanks for reagents which can be refilled, with a 24 hour capacity of each reagent.  Six different wafers can be queued for running, with built-in automation removing spent wafers and swapping in new wafers with new library pools.  


How might the system grow its output?  The patterned wafers place the beads at a very conservative pitch.  Larger diameter wafers are also a possible further option. Extending the read lengths is yet another possible expansion direction.


The instrument has onboard GPU compute power, which is currently used for basecalling and alignment and could ultimately also perform the variant calling work.  


Current accuracy is 0.1% error for substitutions and 0.5% for indels.  Most of the indel error is concentrated in homopolymers greater than 8, with calling capped at 12.  When used with the specially modified GATK co-developed with the Broad, or other custom DeepVariant or Sentieon pipelines, SNP calling accuracy of 99.7% precision, 99.7% recall is achieved and indel recall and precision range from 96-98% for small indels (excluding long homopolymers and low complexity regions).  Accuracy suffers in low complexity regions, which Ultima believes is an amplification chemistry not sequencing chemistry issue and they believe they can significantly improve on the current performance.  


Ultima plans to offer their own kits for PCR-free and PCR-based sheared genomic libraries.  Libraries for other systems can be converted by a simple indexing PCR scheme - this has been done for TruSeq libraries and proof-of-concept experiments have been run for Nextera libraries.  


What could be done with such an instrument?  A pending publication uses Ultima and Illumina in parallel on the same 4 million cell Perturb-Seq experiment and finds the results equivalent between the platforms.  A large fraction of the Phase IV ENCODE HiC data was generated on Ultima.  An internal proof-of-concept experiment utilized deep sequencing RNA from COVID-19 infected samples, recovering complete viral genomes after only ribosomal RNA depletion.  One of the AGBT abstracts demonstrates the ability of Ultima WGS to detect minimal residual disease at low levels by deep WGS of cell-free DNA, an approach academia and startups are actively exploring.  Additional AGBT abstracts describe population genetics studies, oncology, and rare disease sequencing.  Ultima has 10 paying Early Access customers, with 7 instruments installed to date – and these run the gamut from large academic genome centers to biopharma to government labs.  They hope to have “well into double digits” customers at the time of the official launch.


To get here Ultima has raised over $550 million dollars and hired over 350 employees.  The company has made steady progress from their start in 2016.  . Ultima CSO Doron Lipson previously was part of the teams at Helicos and Foundation Medicine, so he has extensive experience both in building a sequencing platform and applying it at scale. CEO Gilad Almogy has spent many years in the semiconductor manufacturing field - Ultima’s reaction wafers are patterned atop silicon substrates and the semiconductor industry also uses very high precision optical methods for both manufacturing and quality control.  


Illumina for a long time now has had an unassailed position as leader in sequencing in the US market as well as others.  Now that position is under pressure from all sides: Element and Singular are trying to squeeze the NextSeq market while Ultima is aiming for the top; Oxford Nanopore thinks their “short fragment mode” can compete as well and the patent shackles are being lifted from BGI.  At JP Morgan in January Illumina said their “Chemistry X” would offer improvements in accuracy, read length and output, but absolutely no details have been forthcoming – and in particular whether new instruments will be required to access Chemistry X benefits.  Perhaps the entry of Ultima and the others will add some urgency to Illumina communicating their future plans, lest customers start planning in earnest to opt for the new platforms


For we consumers of sequence data, more competition and lower prices are a pure good. Projects can continue to be increasingly ambitious and simply the number of different phenomena which can be converted into a sequence measurement constantly grows.  More for less is never, ever going to become boring – it will always be enabling.  After a long period of very shallow slope in the notorious “better than Moore’s Law” slide, we appear to be entering a new period of plunging sequencing costs.  Time to start making plans to take advantage of it!


[20220608 corrected really embarrassing millions typo (should have been billions) which has been requoted all over Twitter]

Monday, May 23, 2022

London Calling 2022: Peptide Sequencing

London Calling was last week and Clive Brown's big revelation was a peek at Oxford Nanopore's progress on enabling peptide sequencing on the platform.  Peptide sequencing and identification is a hot area right now, with multiple startups looking to provide alternatives to mass spectrometry approaches.  Clive stressed that the technology is very early in development.  It's definitely a clever fork of the existing DNA sequencing technology.  However, it also illustrates a significant organizational challenge which Oxford. So I'm going to spend a post focused on this while I figure out how to slice up the rest of the meeting.

Friday, April 15, 2022

Nanopore Knights' Notes

Clive Brown gave a "mezzanine" update on Oxford Nanopore just over two weeks ago titled "The Knights Who Say Me".  Clive reiterated a lot of prior guidance but did make a few announcements that are relevant to the ongoing history of the Oxford Nanopore platform - and blessedly, he omitted for time's sake a deep coverage of that history or the usual Nanopore 101 tutorial.    In particular, two long-time components of the platform are now headed for the exits.

Thursday, March 31, 2022

The End of the Beginning of Human Genome Sequencing?

Today in Science a slew of papers have been published from the Telomere-to-Telomere (T2T) Consortium.  The flagship paper details the generation of a complete genome assembly from a Complete Hydatiform Mole (CHM) cell line which is telomere-to-telomere for all 22 autosomes plus X (assembly T2T-CHM13); the companion papers apply this groundbreaking assembly to a number of biological questions.  PacBio CSO Jonas Korlach and I chatted yesterday about the PacBio contribution to the flagship as well as two of the other papers, as well as another T2T preprint on automated assembly and a related paper from Heng Li and colleagues that recently appeared in Nature Biotechnology.  I did not have advance access to the T2T paper but it had appeared in preprint form and Jonas assured me that no substantial information was added in the published version. 

Monday, March 14, 2022

Element Unveils AVITI

Element Biosciences is launching their AVITI sequencing system today in a blitz of events.  At February’s end they flew me out to visit their San Diego facility and gave me quite amazing access to senior staff, Board of Directors members for an entire day of discussions. They even videotaped me! 


Many of those discussions got deep into technical weeds in a most enjoyable manner.  But for those wishing to jump straight to key details, AVITI is a desktop instrument priced at $289K, a bit below NextSeq 2000, which can run two flowcells entirely independently; two sequencers for the space and outlay of one.  At a cost of $1680  of consumables a user can generate 800 million reads in 2x150 format in 48 hours – or about 5-7 dollars per gigabase if running around specifications.  Element believes their projected yield can be very reliably reached, with many runs over 1 billion reads.  Element disclosed today three beta test sites: HudsonAlpha, the Broad Institute and Stanford.


As I’ll detail farther down, Element has partnered with multiple leading library preparation companies to enable a wide array of sequencing applications and will also offer a kit to convert Illumina libraries.  They’ve also started partnering with bioinformatics tools providers.





Surfaces & Polonies

Let’s start with something I don’t generally think much about: flowcell surfaces.  They’re really, really passionate about “contrast to noise ” at Element, which is basically interchangeable with “signal to noise”.  Whichever way you arrange the equation, it’s about maximizing signal and minimizing non-signal.  And that all starts with a surface.


As they described it, the quest for the perfect surface first means making a surface with absolutely no background - perfectly passivated as they describe it.  So many iterations were tried until they had what seemed like the Vantablack of flowcell surfaces.


But such perfection is a bit of a paradox: just as a non-stick coating must adhere to a pan, the monotonous passivation perfection of the surface must be specifically modified to enable signal to occur.  So further rounds of iteration, trying to provide attachment sites while minimally degrading perfect nothingness.


I asked whether the flowcells is patterned, and it isn’t.  And furthermore any sort of patterning such as wells brings in even more inhomogeneity, more risk of enabling noise to latch on.  Edges and corners are all special and different - and so at risk of generating background signal.  


Once you have attachment sites one must prepare and attach polonies there  So a next challenge was forming polonies in a reliably orderly fashion; it sounds as if Element could fill a modern art gallery with images of polony growth gone awry, but after many iterations a workable polony generation protocol emerged

Library Molecules

Library molecules for AVITI are circles and amplified by a rolling circle mechanism.  Figuring out a paired end chemistry came next, and apparently gave the team great worries that they couldn’t get a robust system to work – but eventually they found one. Element and external collaborators have demonstrated nearly no index hopping and very low polony duplication rates, both sometimes frustrating on Illumina platforms particularly on newer instruments using Exclusion Amplification.


I asked about the insert size range that Element’s polony technology can support.  Element has focused on typical short read library insert sizes of a few hundred bases.  They didn’t believe that very short inserts (such as for micro-RNA or something like Swab-Seq) would be a problem but haven’t explored it.  On the long end they haven’t looked either.


Circular library molecules guarantees not being able to just squirt Illumina libraries on, but Element will offer a conversion kit, albeit with a roughly 2:1 exchange rate unfavorable to Element – if your prep previously made exactly one run’s worth of library you’ll now need twice as much starting material.  But most users will probably take advantage of native kits.  On my visit day  Element announced partnerships with QIAGEN, Agilent, NEB, Roche(Kapa) and Watchmaker for library kits, and in the following days they added Dovetail Genomics and 10X Genomics.  Plus JumpCode Genomic’s ribosomal RNA and other abundant RNA depletion reagents.  So a very wide array of sequencing applications will be natively supported on AVITI from the beginning.


Element also announced recently acquisition of Loop Genomics, which has a synthetic read technology that they sell in two forms.  One kit (Solo)  is intended to replace Sanger sequencing of individual clones and the other works on pools of sequences such as 16S amplicon pools.  Interestingly, Element has no plans to discontinue Loop kits for existing platforms.  The Loop acquisition has also meant less drive to explore longer reads or longer inserts; for these Loop is seen as the solution

Sequencing Chemistry

Once you have a library sprouted as polonies on the flowcell, how does the chemistry work?  It’s an interesting twist on reversible terminator chemistry in which each position is probed twice, once with labels and the polymerase unable to extend and once with unlabeled reversible terminators to march the polony one base forwards.  It also leads to an interesting philosophical question as to whether this is sequencing-by-synthesis.  On one hand single base extension is an integral part of the sequencing cycle; on the other the base extension step is not what generates the signal used to resolve the sequence.  In my own taxonomy, it is definitely cyclic chemistry with optical detection running on clonal molecules sitting on a surface – and I suppose I would vote to create binding as yet another mode since that is the detection step.


The beauty of this polymerase two step is in the labeled nucleotides.  These are not loose nucleotides but rather multiple nucleotides are connected by linkers to a core which in turn is linked to the actual labels.  What’s so clever about this is that each nucleotide interacts extremely weakly with polymerase, since it can’t be covalently linked to the precursor  chain.  So only if many such weak binding events happen will signal occur.  Hence the term “sequencing by avidity.  


These  spider-shaped molecules, which the Element team refers to in conversation as “Avidites” offer many grounds for optimization – linker lengths, number of labels on the Avidite core, etc.  But from a chemical standpoint they’re wonderfully modular, so it’s straightforward to experiment with one section without requiring any synthesis changes on other regions – the chemical equivalent of encapsulation in software engineering. Plus the fluor isn’t up close to the DNA, which means it is less likely to generate any sort of photodamage.


Since one is relying on  Avidites aggregating many small interactions into a large net interaction, the concentration of  Avidites need not be very high – nanomolar versus micromolar levels more typical for sequencing reagents.  That means less expensive reagent being used in each cycle - comment was made that in typical sequencing reactions the color of reagent going in is same as that of the waste because only an infinitesimal amount of reagent is actually incorporated into  growing strands.  Low concentrations  also means less likelihood of reagent sticking non-specifically to the flowcell.


One consequence of the avidity approach  is that loss of phase results in only a very weak and slow growing background.  Particularly in early cycles, within each polony dephased molecules will be few and on average widely separated.  Hence wrong Avidite arms won’t make sufficient interactions to loiter and be detected.


At this time Element is offering only 2x150 kits, but with Q40 early in the read gliding down to Q30 at 150 bases.  I asked if they could go longer: CEO Molly He replied that they think the core market is centered on 2x150 but they will monitor demand.   Molly thinks Element is only at the beginning of exploring the new Avidity chemistry with many avenues to explore to obtain significant further optimization.  With the existing quality score pattern, I do wonder if there are some select applications - such as sequencing long simple repeats for repeat expansion disorder research - that could leverage much longer reads using Element’s chemistry.


A single chemistry kit means a streamlined inventory for Element and for customers.  It is indeed nice to be able to save money by ordering less expensive kits for applications that require less data, but often those savings evaporate when you find yourself with a glut of about to expire kits that don’t match your immediate applications.  Actual read lengths can be adjusted in software and there will also be an option to scan only portions of the two channel flowcell to shorten total run time.  CEO Molly He also believes that overall runtime can be shortened; it is set conservatively for a smooth launch but further optimization might shave time off each cycle.


Remarkably this all came together quickly, about 4 years from first acquiring lab space to an externally validated DNA sequencer.This included some nice breaks such as writing specifications for a camera and then inventing a much better one with a wider field of view and with less distortion around the edges than had been originally anticipated, enabling more polonies to be imaged with each exposure.  Element also developed  a new primary analysis algorithm for highly  accurate base-calling of high density polonies.


Element is keeping most consumable manufacturing in house.  Growth has led to three sites in the La Jolla area and one research station in the Bay Area, but the La Jolla sites will soon be consolidated to a single 80 thousand square foot building nearly completion.  The new building will enable manufacturing reagents in much larger batches.  And while the instrument has been launched as Research Use Only, manufacturing data systems are being built with GxP concepts in mind for the future, as well as the value of rich data for troubleshooting manufacturing issues.


As with essentially every sequencing technology company, and reflecting CEO Molly He’s background in the field, Element has a large investment in protein engineering.  AVITI  sports three different polymerases, each optimized for its role in the process.  So one polymerase for polony formation, one polymerase for detection-by-avidity and one for extending with reversible terminator.  


Data

On the data side, AVITI emits industry-standard FASTQ.  Demultiplexing of barcodes is performed off instrument.  Element wants to enable users to interface with any desired bioinformatics platform, cloud or not.  They have been announcing partnerships in this space – with Google DeepVariant and Sentieon for AVITI-tuned variant calling models, Genoox for rare disease research, and Fabric Genomics for clinical variant interpretation. 


The application note from Watchmaker shows excellent uniformity across the range of GC content found in a human sample 

HudsonAlpha data showed by Shawn Levy suggests that AVITI is superior to Illumina for small indel calling but slightly worse overall - but pay attention to those Y axis ticks - it’s about 0.4 percentage points different (though the failure to downsample to same depth for this slide  makes the comparison dicey).

Market Strategy

In terms of competing with the entrenched market leader, Element is counting on some marketplace judo.  The thinking is this: Illumina’s real focus is on NovaSeq in huge sequencing factories; that’s their main driver of revenue.  AVITI will be aimed right around the overlap between the NextSeq 2000 and the bottom of NovaSeq performance (SP flowcell), but cutting under the list price of NextSeq and offering a lower (list) consumable option . And that’s not a small amount lower - based on the list pricing for NextSeq reagents currently in Albert Vilella’s wonderful  NGS comparison spreadsheet, AVITI with delivers twice the output of a P2 flowcell (800M 2x150 reads vs 400M)  for 47% of the price ($1680 vs. $3800) - so about 4X improvement in price vs. performance!  NextSeq P3 flowcells are specified to have 50% more data than AVITI, but the price/performance ratio is around 2-fold (5-7 dollars per gigabase vs. 10.5 for P3).  Of course, real values depend on field performance and whatever pricing Illumina grants an organization.   Presumably Illumina could give up some margin on NextSeq to compete, but they risk disincentivizing labs upgrading to NovaSeq if the NextSeq becomes too favorable for smaller jobs - and the NovaSeq margins are too important to be touched  That’s one thesis Element is working from. Element’s belief is that “decentralized sequencing will enable more scientists and clinicians to accelerate their learning without compromising cost and quality”. 

 

Another marketing thought is lifted from the Innovator’s Dilemma: the idea is that NovaSeq really overshoots the performance needs of most labs but there is a sizable market, particularly with core facilities, for a more modestly-priced instrument that offers flexible operation but enough data to satisfy common academic sequencing experiments. NovaSeq’s temptingly low cost per base only works if you are running it in the high output modes and if those bases really are useful, and many core labs have trouble filling flow cells in a timely manner.  Not only is the NovaSeq (list) about three fold the price of AVITI, but that also means the annual service contract in following years will also be about three fold higher.   There’s also of course a feeling that the genomics field strongly desires some effective competition for Illumina in core markets and there is pent up demand for an alternative.


Element will be implementing transparent, uniform pricing.  There will be volume discounts available, but the same ones for all – no haggling to try to get a better price only to discover you’re not as good at haggling as you think.  Also good for people like me who (a) hate haggling and (b) want to be able to compare prices without worrying that reality is very different than sticker prices.


Will Element Succeed?

When I was visiting I really was taken by the focused intensity of the technical team and the enthusiasm of the leadership team – which included discussions with Board members (and industry veterans)  Jim Tannanbaum and John Stuelpnagel.  John, for example, catalyzed the formation of Illumina and was on its board for many years; since then he’s started or been on the board a range of genomics-focused companies in microfluidic library prep (10X Genomics), non-invasive pre-natal testing (Ariosa), immunosequencing (Sequenta) and genome editing (Inscripta).  Jim’s resume overlaps with 10X, but has been more pharmaceutical focused: Jazz Pharmaceuticals, Innoviva, Theravance, and GelTex   Both described in careful detail their excitement with Element’s technology and their satisfaction with how Element’s team has executed on developing that technology.   On the applications side Element has snagged as a senior vice president Shawn Levy, well known for road testing new sequencing platforms and technologies during his tenure at HudsonAlpha Institute.  So they have a huge base of talent and expertise to drive the launch into the sequencing market.


Will this all work out for Element?  As I discussed earlier in the year, there are multiple companies jumping into the short read market over the next year or so.  Singular plans to launch in early summer, BGI should be free of patent constraints by late summer and PacBio plans to launch Omniome technology sometime next year.  Oxford Nanopore wants to play in this space too, though to say their reads are different in quality than Element’s is a bit of an understatement.  Illumina promises higher qualities with Chemistry X, though without any details as to when this chemistry will launch and complete uncertainty whether it will be part of a new fleet of instruments.  And perhaps there are other new entrants flying under the radar.


Given all that, Element will must execute nearly flawlessly in locking down some customers, getting instruments and consumables to customers, dealing efficiently and in a forthright manner with the inevitable hiccups as instruments enter the field and generating increasing buzz at meetings such as the different incarnations of AGBT.  Independent confirmation of their read quality claims on a variety of different inputs will be something to watch for, particularly on challenging targets such as extremes of %GC, long homopolymers, long VNTR repeats (such as in triplet expansion disorders), and strong hairpin-prone structures.


Stay tuned.  Watching Element execute promises to be interesting.


[20220315 06:16 fixed homogeneity --> inhomogeneity ]


Thursday, February 17, 2022

Pro Tip: Customer Hostile is Never A Good Look

A bizarre incident happened on Twitter yesterday.  Someone contemplating using Oxford Nanopore to sequence a large, complex genome on a tight budget was asking technical questions about whether to optimize their libraries for overall yield or long inserts, and was getting useful advice from some of the top academic scientists who have propelled ONT forward.  One of them suggested using Circulomics products, and that was followed by an ominous yet vague warning from an ONT employee.  But not just any ONT employee, but Chief Strategy Officer Spike Willcocks.  Having not seen a retraction of that tweet, I'm here to point out just how self-defeating the warning is.

Tuesday, February 15, 2022

Parse Bio Pools Further Funding

Seattle-based single cell analysis firm Parse Bio is announcing this morning a $41.5M Series B round of funding, pushing their total raise just over $50M.  Parse uses chemical fixation to lock biomolecules onto their enclosing cells or nuclei, which can then be manipulated without releasing their contents.  This enables a series of split-label-pool operations to tag the molecules of interest with barcodes so that in the end each cell has a unique barcode.  The protocol requires no specialized instrument, enables collecting samples over different timepoints while quenching changes in gene expression and can scale to very high cell numbers. Co-founders Alex Rosenberg and Charlie Roco sat down with me over Zoom last week to review the company and their technology.

Monday, January 31, 2022

Notes from a Conversation with PacBio's Christian Henry

PacBio CEO Christian Henry was kind enough to chat with me by videoconference just after JP Morgan.  To get the the obvious issue out of the way, let me say that while it is common to agree to meet with interview subjects at some future date when they are in Boston, he is the first one to suggest he would just stop by my desk and we'd head to a break room.  Henry sits on my employer's board, so if you think that shades my opinions you are forewarned.

Monday, January 17, 2022

Could Hercule Poirot Crack The Case of Genapsys' Business Strategy?

If you love a good mystery, let me try to draw you in to the enigma of Genapsys' business strategy.  Genapsys presented last week at J.P. Morgan, but nobody who wasn't there knows what they said or presented.  Keeping their future plans hush-hush is a strange course for a company that hasn't caught fire and is about to face multiple well-funded new competition.

Wednesday, January 12, 2022

Illumina Teases Two Glittering Enigmas

Illumina's J.P. Morgan presentation was largely focused on various applications of their platform.  But on the further platform development side, they did throw out two new products as very, very limited descriptions: Chemistry X as the future of sequencing-by-synthesis and Infinity for 10 kilobase synthetic reads.  Both have triggered a lot of speculation and indeed some very clever sleuthing, since neither really had anything but the faintest of details provided

Tuesday, January 11, 2022

Apologies & A Vow To Do Better

To my readers: I am quite embarrassed by the multiple errors which were present in the first two postings of the year, which include incomplete sentences in jumbled paragraphs, small but key errors of fact and writing "short read" in a key place where I meant "long read'. They are the sort of errors I can be quite harsh on others making.  I put too much emphasis on pushing these out and far, far too little on proofreading and reviewing them.  You deserve better.

Thursday, January 06, 2022

Three Reactions from December's PacBio+Invitae Mendelspod



Theral Timpson hosted PacBio CEO Christian Henry and Invitae CEO Sean George for a Mendelspod podcast  back on Pearl Harbor day last month.  It's a fun, chatty interview with the two which illustrated why these two companies have an excellent strategic fit.  I won't summarize all of it, but I did have strong reactions to three points

Monday, January 03, 2022

2022: A Wild Year for Short Reads?

It looks like 2022 might be an exciting year for the short read genomics market, with new players taking on Illumina.  J.P. Morgan will be virtual next week, so perhaps some of the players will make some announcements.  Here's some thoughts on the situation as it stands now in a space where many of failed before -- QIAGEN, ThermoFisher (SOLiD) and Roche(454) -- as well as some have bailed out before even entering -- Agilent.