Evidence map›Paper›PMID 29790906›Full record

ArticleBioinformatics (Oxford, England)2018

bcSeq: an R package for fast sequence mapping in high-throughput shRNA and CRISPR screens.

Jiaxing Lin, Jeremy Gresham, Tongrong Wang, So Young Kim, James Alvarez, Jeffrey S Damrauer, Scott Floyd, Joshua Granek, Andrew Allen, Cliburn Chan and 2 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Cooperative regulation of coupled oncoprotein synthesis and stability in triple-negative breast cancer by EGFR and CDK12/13.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  3. 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

12 authors.

Jiaxing LinBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.
Jeremy GreshamDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
Tongrong WangBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.
So Young KimMolecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
James AlvarezDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
Jeffrey S DamrauerLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Scott FloydDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
Joshua GranekBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.
Andrew AllenBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.
Cliburn ChanBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.
Jichun XieBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.
Kouros OwzarBiostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA.

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVIDIAN, MARIE, KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Targeted Alpha-Particle Radiotheraphy of Brain Tumors with 211At-81C6 AntibodyP50CA190991 · NCI · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2014 to 2023
$20.8M
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
NCI NIH HHS P01 CA142538NCI NIH HHS P50 CA190991NIH HHS S10 OD018164
6 · The paper itself

Abstract

Summary: CRISPR-Cas9 and shRNA high-throughput sequencing screens have abundant applications for basic and translational research. Methods and tools for the analysis of these screens must properly account for sequencing error, resolve ambiguous mappings among similar sequences in the barcode library in a statistically principled manner, and be computationally efficient. Herein we present bcSeq, an open source R package that implements a fast and parallelized algorithm for mapping high-throughput sequencing reads to a barcode library while tolerating sequencing error. The algorithm uses a Trie data structure for speed and resolves ambiguous mappings by using a statistical sequencing error model based on Phred scores for each read. Availability and implementation: The package source code and an accompanying tutorial are available at http://bioconductor.org/packages/bcSeq/. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsClustered Regularly Interspaced Short Palindromic RepeatsGene LibraryHigh-Throughput Nucleotide SequencingRNA, Small InterferingSoftwareRNA, Small Interfering

Identifiers

PMID29790906
PMCPMC6184561

What OpenQuestion holds

Textmetadata
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.