(Q30841251)

7 November 2017

Identification of copy number variants from exome sequence data (English)

1 reference

7 November 2017

Geir Erland Tjønnfjord

6

object named as

Geir E Tjønnfjord

1 reference

7 November 2017

Pubudu Saneth Samarakoon

1

1 reference

7 November 2017

Hanne Sørmo Sorte

2

1 reference

7 November 2017

Bjørn Evert Kristiansen

3

1 reference

7 November 2017

Tove Skodje

4

1 reference

7 November 2017

Ying Sheng

5

1 reference

7 November 2017

Barbro Stadheim

7

1 reference

7 November 2017

Asbjørg Stray-Pedersen

8

1 reference

7 November 2017

Olaug Kristin Rødningen

9

1 reference

7 November 2017

Robert Lyle

10

1 reference

7 November 2017

language of work or name

English

0 references

publication date

7 August 2014

1 reference

7 November 2017

1 reference

7 November 2017

15

1 reference

7 November 2017

661

1 reference

Modeling read counts for CNV detection in exome sequencing data

7 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

GENCODE: the reference human genome annotation for The ENCODE Project

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

A robust model for read count data in exome sequencing experiments and implications for copy number variant calling

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Copy number variation detection and genotyping from exome sequence data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

The 1000 Genomes Project: data management and community access

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

CONTRA: copy number analysis for targeted resequencing

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Exome sequencing as a tool for Mendelian disease gene discovery

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

A framework for variation discovery and genotyping using next-generation DNA sequencing data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Resolving the resolution of array CGH.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

A faster circular binary segmentation algorithm for the analysis of array CGH data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Detection of clinically relevant copy number variants with whole-exome sequencing.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4132917

Genetic subtyping of Fanconi anemia by comprehensive mutation screening

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25102989

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-15-661

1 reference

Dimensions Publication ID

7 November 2017

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2164-15-661

1 reference

7 November 2017

PubMed publication ID

25102989

1 reference