(Q46183708)

20 December 2017

title

Variant Review with the Integrative Genomics Viewer (English)

1 reference

20 December 2017

0 references

0 references

5

Jill P Mesirov

1 reference

20 December 2017

Helga Thorvaldsdóttir

2

object named as

Helga Thorvaldsdóttir

0 references

author name string

James T Robinson

1

1 reference

20 December 2017

Helga Thorvaldsdóttir

2

1 reference

20 December 2017

Aaron M Wenger

3

1 reference

20 December 2017

Ahmet Zehir

4

1 reference

20 December 2017

language of work or name

English

0 references

publication date

1 November 2017

1 reference

20 December 2017

published in

Cancer Research

1 reference

20 December 2017

volume

77

1 reference

20 December 2017

issue

21

1 reference

20 December 2017

page(s)

e31-e34

1 reference

20 December 2017

Current practices and guidelines for clinical next-generation sequencing oncology testing

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Resolving the complexity of the human genome using single-molecule sequencing

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Integrated analysis of germline and somatic variants in ovarian cancer.

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Integrative genomics viewer

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

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

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

The Sequence Alignment/Map format and SAMtools

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

Real-time DNA sequencing from single polymerase molecules

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

BLAT—The BLAST-Like Alignment Tool

29 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5678989

10.1158/0008-5472.CAN-17-0337

29 September 2018

Identifiers

DOI

1 reference

20 December 2017

PMC publication ID

5678989

0 references

1 reference

20 December 2017