(Q34194748)

31 July 2017

title

In-depth annotation of SNPs arising from resequencing projects using NGS-SNP (English)

1 reference

31 July 2017

Paul Stothard

1 reference

31 July 2017

Jason R Grant

1 reference

31 July 2017

Adriano S Arantes

series ordinal

1 reference

31 July 2017

Xiaoping Liao

series ordinal

1 reference

31 July 2017

language of work or name

English

0 references

publication date

22 June 2011

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

31 July 2017

page(s)

2300-2301

1 reference

Creative Commons Attribution-NonCommercial 2.5 Generic

31 July 2017

start time

2 October 2016

1 reference

April 2023 Public Data File from Crossref

copyrighted

0 references

cites work

Entrez Gene: gene-centered information at NCBI

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

Ongoing and future developments at the Universal Protein Resource

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

SeqAnt: a web service to rapidly identify and annotate DNA sequence variations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

KEGG for representation and analysis of molecular networks involving diseases and drugs

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

The Sequence Alignment/Map format and SAMtools

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150039

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.

28 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR372

Mapping short DNA sequencing reads and calling variants using mapping quality scores

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR372

CandiSNPer: a web tool for the identification of candidate SNPs for causal variants

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTR372

10.1093/BIOINFORMATICS/BTR372

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/GrantALS11

31 July 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

31 July 2017

1 reference