Evidence map›Paper›PMID 30837529›Full record

ArticleScientific reports2019

CRISPR/CAS9 targeted CAPTURE of mammalian genomic regions for characterization by NGS.

Alexei Slesarev, Lakshmi Viswanathan, Yitao Tang, Trissa Borgschulte, Katherine Achtien, David Razafsky, David Onions, Audrey Chang, Colette Cote

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

19 citing papers in PubMed, 36 citations in OpenAlex.

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  15. Versatile 3' Functionalization of CRISPR Single Guide RNA.Chembiochem : a European journal of chemical biology · 2020
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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

9 authors at 1 institution in 1 country.

Alexei SlesarevBioReliance Corp., 14920 Broschart Road, Rockville, MD, 20850, USA. alexei.slesarev@sial.com.
Lakshmi ViswanathanBioReliance Corp., 14920 Broschart Road, Rockville, MD, 20850, USA.
Yitao TangBioReliance Corp., 14920 Broschart Road, Rockville, MD, 20850, USA.
Trissa BorgschulteMilliporeSigma, 2909 Laclede Avenue, Saint Louis, MO, 63103, USA.
Katherine AchtienMilliporeSigma, 2909 Laclede Avenue, Saint Louis, MO, 63103, USA.
David RazafskyMilliporeSigma, 2909 Laclede Avenue, Saint Louis, MO, 63103, USA.
David OnionsBioReliance Corp., 14920 Broschart Road, Rockville, MD, 20850, USA.
Audrey ChangBioReliance Corp., 14920 Broschart Road, Rockville, MD, 20850, USA.
Colette CoteBioReliance Corp., 14920 Broschart Road, Rockville, MD, 20850, USA.
BioReliance (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The robust detection of structural variants in mammalian genomes remains a challenge. It is particularly difficult in the case of genetically unstable Chinese hamster ovary (CHO) cell lines with only draft genome assemblies available. We explore the potential of the CRISPR/Cas9 system for the targeted capture of genomic loci containing integrated vectors in CHO-K1-based cell lines followed by next generation sequencing (NGS), and compare it to popular target-enrichment sequencing methods and to whole genome sequencing (WGS). Three different CRISPR/Cas9-based techniques were evaluated; all of them allow for amplification-free enrichment of target genomic regions in the range from 5 to 60 fold, and for recovery of ~15 kb-long sequences with no sequencing artifacts introduced. The utility of these protocols has been proven by the identification of transgene integration sites and flanking sequences in three CHO cell lines. The long enriched fragments helped to identify Escherichia coli genome sequences co-integrated with vectors, and were further characterized by Whole Genome Sequencing (WGS). Other advantages of CRISPR/Cas9-based methods are the ease of bioinformatics analysis, potential for multiplexing, and the production of long target templates for real-time sequencing.

Indexed as

CRISPR-Cas SystemsGene EditingGenomeAnimalsCHO CellsChromosome MappingCricetinaeCricetulusHigh-Throughput Nucleotide SequencingMammals

Identifiers

PMID30837529
PMCPMC6401131
OpenAlexW2949254233

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.