Development and validation of the JAX Cancer Treatment Profile™ for detection of clinically actionable mutations in solid tumors. (Q35538750)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25562415%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

title

Development and validation of the JAX Cancer Treatment Profile™ for detection of clinically actionable mutations in solid tumors (English)

1 reference

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27 February 2020

8

1 reference

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27 February 2020

14

Carol Bult

1 reference

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27 February 2020

author name string

Guruprasad Ananda

1

1 reference

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27 February 2020

Susan Mockus

2

1 reference

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27 February 2020

Micaela Lundquist

3

1 reference

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27 February 2020

Vanessa Spotlow

4

1 reference

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27 February 2020

Al Simons

5

1 reference

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27 February 2020

Talia Mitchell

6

1 reference

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27 February 2020

Grace Stafford

7

1 reference

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27 February 2020

Timothy Stearns

9

1 reference

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27 February 2020

Anuj Srivastava

10

1 reference

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27 February 2020

Mary Barter

11

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27 February 2020

Lucy Rowe

12

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27 February 2020

Joan Malcolm

13

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27 February 2020

Radha Krishna Murthy Karuturi

15

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27 February 2020

Karen Rasmussen

16

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27 February 2020

Douglas Hinerfeld

17

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27 February 2020

publication date

3 January 2015

1 reference

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Experimental and Molecular Pathology

27 February 2020

published in

1 reference

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27 February 2020

volume

98

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27 February 2020

page(s)

106-112

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27 February 2020

issue

1

1 reference

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The Cancer Genomics Resource List 2014.

27 February 2020

cites work

1 reference

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Validation of a next-generation-sequencing cancer panel for use in the clinical laboratory.

12 July 2018

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Theranostic Profiling for Actionable Aberrations in Advanced High Risk Osteosarcoma with Aggressive Biology Reveals High Molecular Diversity: The Human Fingerprint Hypothesis

12 July 2018

1 reference

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Navigating the rapids: the development of regulated next-generation sequencing-based clinical trial assays and companion diagnostics

12 July 2018

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Where cancer genomics should go next: a clinician's perspective

12 July 2018

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Enabling a genetically informed approach to cancer medicine: a retrospective evaluation of the impact of comprehensive tumor profiling using a targeted next-generation sequencing panel

12 July 2018

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Profiling cancer gene mutations in clinical formalin-fixed, paraffin-embedded colorectal tumor specimens using targeted next-generation sequencing

12 July 2018

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Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

12 July 2018

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Routine use of the Ion Torrent AmpliSeq™ Cancer Hotspot Panel for identification of clinically actionable somatic mutations

12 July 2018

1 reference

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Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4481190

KRAS as prognostic biomarker in metastatic colorectal cancer patients treated with bevacizumab: a pooled analysis of 12 published trials

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4481190

Clinical validation of a next-generation sequencing screen for mutational hotspots in 46 cancer-related genes.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4481190

P53 mutations in advanced cancers: clinical characteristics, outcomes, and correlation between progression-free survival and bevacizumab-containing therapy

12 July 2018

1 reference

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An integrated map of genetic variation from 1,092 human genomes

12 July 2018

1 reference

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Feasibility of real time next generation sequencing of cancer genes linked to drug response: results from a clinical trial

12 July 2018

1 reference

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High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing

12 July 2018

1 reference

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CONTRA: copy number analysis for targeted resequencing

12 July 2018

1 reference

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ConReg-R: Extrapolative recalibration of the empirical distribution of p-values to improve false discovery rate estimates

12 July 2018

1 reference

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A framework for variation discovery and genotyping using next-generation DNA 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=4481190

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA 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=4481190

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

12 July 2018

1 reference

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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=4481190

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4481190

Validation of a next-generation sequencing assay for clinical molecular oncology.

26 September 2018

1 reference

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Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4481190

10.1016/J.YEXMP.2014.12.009

26 September 2018

Identifiers

DOI

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release_harynwunojf3hbj6dsh4ni5vgi

27 February 2020

Fatcat ID

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mapped directly with Wikidata item

24 November 2022

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27 February 2020

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