Performance comparison of four commercial human whole-exome capture platforms (Q35734002)

10 August 2017

Performance comparison of four commercial human whole-exome capture platforms (English)

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10 August 2017

5

Keith A Boroevich

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10 August 2017

8

Michiaki Kubo

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10 August 2017

9

Tatsuhiko Tsunoda

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10 August 2017

Daichi Shigemizu

1

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10 August 2017

Yukihide Momozawa

2

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10 August 2017

Testuo Abe

3

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10 August 2017

Takashi Morizono

4

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10 August 2017

Sadaaki Takata

6

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10 August 2017

Kyota Ashikawa

7

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10 August 2017

language of work or name

English

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publication date

3 August 2015

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10 August 2017

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10 August 2017

5

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10 August 2017

12742

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Creative Commons Attribution 4.0 International

10 August 2017

start time

3 August 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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exact match

https://scigraph.springernature.com/pub.10.1038/srep12742

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cites work

Performance comparison of four exome capture systems for deep sequencing

1 reference

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A practical method to detect SNVs and indels from whole genome and exome sequencing data

12 July 2018

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

12 July 2018

1 reference

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Exome sequencing and the genetic basis of complex traits

12 July 2018

1 reference

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The 1000 Genomes Project: data management and community access

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

An integrative variant analysis suite for whole exome next-generation sequencing data

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

A comparative analysis of exome capture

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Comprehensive comparison of three commercial human whole-exome capture platforms

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Comparison of solution-based exome capture methods for next generation sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Performance comparison of exome DNA sequencing technologies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Exome sequencing of head and neck squamous cell carcinoma reveals inactivating mutations in NOTCH1

12 July 2018

1 reference

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Exome sequencing reveals comprehensive genomic alterations across eight cancer cell lines

12 July 2018

1 reference

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Exome sequencing identifies GRIN2A as frequently mutated in melanoma

12 July 2018

1 reference

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Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

12 July 2018

1 reference

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

12 July 2018

1 reference

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Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing

12 July 2018

1 reference

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Sequencing technologies - the next generation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Exome sequencing identifies the cause of a mendelian disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

The Sequence Alignment/Map format and SAMtools

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Fast and accurate short read alignment with Burrows-Wheeler transform

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Next-generation DNA sequencing methods

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

Primer: Sequencing--the next generation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4522667

12 July 2018

Identifiers

DOI

10.1038/SREP12742

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10 August 2017

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10 August 2017

1 reference