(Q34095905)

31 July 2017

Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data (English)

1 reference

Isabelle Janoueix-Lerosey

31 July 2017

7

Isabelle Janoueix-Lerosey

0 references

Valentina Boeva

Valentina Boeva

1

0 references

Emmanuel Barillot

Emmanuel Barillot

9

0 references

Olivier Delattre

Olivier Delattre

8

0 references

Gudrun Schleiermacher

6

Gudrun Schleiermacher

1 reference

31 July 2017

3

Kevin Bleakley

1 reference

31 July 2017

5

Julie Cappo

1 reference

31 July 2017

Tatiana Popova

2

1 reference

PubMed ID

22155870

31 July 2017

Pierre Chiche

4

1 reference

PubMed ID

22155870

31 July 2017

language of work or name

English

0 references

publication date

6 December 2011

1 reference

31 July 2017

1 reference

31 July 2017

28

1 reference

31 July 2017

423-425

1 reference

31 July 2017

3

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

31 July 2017

start time

2 October 2016

1 reference

April 2023 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

massive parallel sequencing

1 reference

based on heuristic

inferred from title

cites work

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268243

Hallmarks of Cancer: The Next Generation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268243

Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268243

High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268243

Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268243

dbSNP: the NCBI database of genetic variation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268243

An approach to analysis of large-scale correlations between genome changes and clinical endpoints in ovarian cancer

5 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22155870

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTR670

1 reference

journals/bioinformatics/BoevaPBCCSJDB12

31 July 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

31 July 2017

1 reference

PubMed ID

22155870