Evidence map›Paper›PMID 40461965›Full record

ArticleBMC genomics2025

Flexible, production-scale, human whole genome sequencing on a benchtop sequencer.

Kevin Green, Benjamin Krajacich, Kelly Wiseman, Peter T Mains, Samantha Robertson, Sophie Billings, Marina McCowin, Mitch Sudkamp, Ching Shing Lo, Bryan R Lajoie and 3 more

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Kevin GreenElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Benjamin KrajacichElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Kelly WisemanElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Peter T MainsElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Samantha RobertsonElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Sophie BillingsElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Marina McCowinElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Mitch SudkampElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Ching Shing LoElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Bryan R LajoieElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Semyon KruglyakElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Shawn LevyElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA.
Junhua ZhaoElement Biosciences, 10055 Barnes Canyon Rd. Suite 100, San Diego, CA, 92121, USA. jzhao@elembio.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human whole-genome sequencing (hWGS) provides comprehensive genomic information that can help guide research in disease prevention and treatment. Recent advancements in sequencing technology have improved sequencing quality and further reduced sequencing costs on bench-top sized instruments, making whole-genome sequencing an accessible technology for broader use. Here, we demonstrate the feasibility of a large WGS project using a benchtop sequencer in a small laboratory setting, on a scale previously reserved for production-scale machines. In this project, 807 samples were prepared and sequenced across 313 flow cells, with high sequencing quality at a median %Q30 of 96.6% and a median %Q40 of 89.31%. To screen library quality and maximize sample yield, we utilized 48-plex sample pre-pool 'QC' runs to provide > 1 × coverage per sample prior to sample pooling and full-depth sequencing, providing valuable sample-level insights prior to full-depth sequencing. With this strategy, we consistently achieved > 30 × human whole genome sequencing of three-plex sample trios with standard settings. To demonstrate additional flexibility present in the platform, we explored two different use cases 1) large insert sizes (1kb +) library to achieve superior genome coverage; 2) proof of concept rapid WGS sequencing to minimize sample to answer turnaround time for time-critical sequencing applications. Sequencing of a 2 × 100 > 30 × human WGS can be achieved in < 12 h and subsequent file generation in < 1 additional hour. This study provides a cost-effective and flexible real-world demonstration of achieving both high quality hWGS sequencing and instrument flexibility without the need for complex batching schemes or factory-sized sequencers.

Indexed as

Genome, HumanHigh-Throughput Nucleotide SequencingWhole Genome SequencingGene LibraryHumansBenchmarkingBench Top SequencerGenomicsHigh-Throughput SequencingHuman Whole Genome SequencingRapid Whole Genome SequencingSequencing

Identifiers

PMID40461965
PMCPMC12135483

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.