(Q40762147)

23 September 2017

Novel scripts for improved annotation and selection of variants from whole exome sequencing in cancer research (English)

1 reference

23 September 2017

7

1 reference

23 September 2017

Marcus Celik Hansen

1

0 references

Charlotte G Nyvold

object named as

Charlotte Guldborg Nyvold

series ordinal

6

0 references

Eigil Kjeldsen

series ordinal

5

object named as

Eigil Kjeldsen

1 reference

23 September 2017

3

Anne Roug

1 reference

23 September 2017

2

Line Nederby

1 reference

23 September 2017

Palle Villesen

4

1 reference

23 September 2017

12 March 2015

1 reference

23 September 2017

1 reference

23 September 2017

2

1 reference

23 September 2017

145-153

1 reference

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples

23 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

Gene-disease network analysis reveals functional modules in mendelian, complex and environmental diseases

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

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

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

A method and server for predicting damaging missense mutations

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

Fast and accurate short read alignment with Burrows-Wheeler transform

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

The human genome browser at UCSC

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

dbSNP: the NCBI database of genetic variation

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

Nature and nurture: a case of transcending haematological pre-malignancies in a pair of monozygotic twins adding possible clues on the pathogenesis of B-cell proliferations.

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4487347

10.1016/J.MEX.2015.03.003

19 August 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference

PMC publication ID

4487347

23 September 2017

PubMed publication ID

26150983

1 reference

PMC publication ID

4487347