A practical guide for the functional annotation of genetic variations using SNPnexus (Q46668916)

24 December 2017

title

A practical guide for the functional annotation of genetic variations using SNPnexus (English)

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24 December 2017

author

Nick R Lemoine

series ordinal

2

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24 December 2017

Claude Chelala

object named as

Claude Chelala

series ordinal

3

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author name string

Abu Z Dayem Ullah

series ordinal

1

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24 December 2017

publication date

8 February 2013

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24 December 2017

Briefings in Bioinformatics

published in

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24 December 2017

volume

14

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page(s)

437-447

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issue

4

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24 December 2017

The value of gene-based selection of tag SNPs in genome-wide association studies.

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

dbSNP: the NCBI database of genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

21 January 2018

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21 January 2018

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The vertebrate genome annotation (Vega) database

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AceView: a comprehensive cDNA-supported gene and transcripts annotation

21 January 2018

1 reference

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H-InvDB in 2009: extended database and data mining resources for human genes and transcripts

21 January 2018

1 reference

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The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

21 January 2018

1 reference

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

21 January 2018

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A method and server for predicting damaging missense mutations

21 January 2018

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The TRANSFAC system on gene expression regulation.

21 January 2018

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Prediction of mammalian microRNA targets

21 January 2018

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miRBase: integrating microRNA annotation and deep-sequencing data

21 January 2018

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snoRNA-LBME-db, a comprehensive database of human H/ACA and C/D box snoRNAs

21 January 2018

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CpG islands in vertebrate genomes

21 January 2018

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In vivo enhancer analysis of human conserved non-coding sequences

21 January 2018

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Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

21 January 2018

1 reference

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The genetic association database

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

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

21 January 2018

1 reference

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

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Structural variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

Detection of large-scale variation in the human genome

21 January 2018

1 reference

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Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.

21 January 2018

1 reference

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TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study

21 January 2018

1 reference

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REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIB%2FBBT004

21 January 2018

Identifiers

DOI

10.1093/BIB/BBT004

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24 December 2017

DBLP publication ID

journals/bib/UllahLC13

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DBLP Dataset 2021-01-02

28 January 2021

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24 December 2017