Evidence map›Paper›PMID 28432350›Full record

ArticleScientific reports2017

Enhancing the throughput and multiplexing capabilities of next generation sequencing for efficient implementation of pooled shRNA and CRISPR screens.

Md Fahmid Islam, Atsushi Watanabe, Lai Wong, Conor Lazarou, Frederick S Vizeacoumar, Omar Abuhussein, Wayne Hill, Maruti Uppalapati, C Ronald Geyer, Franco J Vizeacoumar

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Md Fahmid IslamDepartment of Biochemistry, University of Saskatchewan, Saskatoon, S7N 5E5, Canada.
Atsushi WatanabeDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada.
Lai WongDepartment of Biochemistry, University of Saskatchewan, Saskatoon, S7N 5E5, Canada.
Conor LazarouDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada.
Frederick S VizeacoumarDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada.
Omar AbuhusseinCollege of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, S7N 5C9, Canada.
Wayne HillDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada.
Maruti UppalapatiDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada.
C Ronald GeyerDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada. ron.geyer@usask.ca.
Franco J VizeacoumarDepartment of Pathology, University of Saskatchewan, Saskatoon, S7N 0W8, Canada. franco.vizeacoumar@usask.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next generation sequencing is becoming the method of choice for functional genomic studies that use pooled shRNA or CRISPR libraries. A key challenge in sequencing these mixed-oligo libraries is that they are highly susceptible to hairpin and/or heteroduplex formation. This results in polyclonal, low quality, and incomplete reads and reduces sequencing throughput. Unfortunately, this challenge is significantly magnified in low-to-medium throughput bench-top sequencers as failed reads significantly perturb the maximization of sequence coverage and multiplexing capabilities. Here, we report a methodology that can be adapted to maximize the coverage on a bench-top, Ion PGM System for smaller shRNA libraries with high efficiency. This ligation-based, half-shRNA sequencing strategy minimizes failed sequences and is also equally amenable to high-throughput sequencers for increased multiplexing. Towards this, we also demonstrate that our strategy to reduce heteroduplex formation improves multiplexing capabilities of pooled CRISPR screens using Illumina NextSeq 500. Overall, our method will facilitate sequencing of pooled shRNA or CRISPR libraries from genomic DNA and maximize sequence coverage.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsFlavonoidsHEK293 CellsHigh-Throughput Nucleotide SequencingHumansRNA, Small InterferingSequence Analysis, RNAFlavonoidsprimetinRNA, Small Interfering

Identifiers

PMID28432350
PMCPMC5430825

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.