(Q30652002)

17 August 2017

Approaches to the detection of recessive effects using next generation sequencing data from outbred populations (English)

1 reference

17 August 2017

David Curtis

1

0 references

publication date

11 June 2013

1 reference

Advances and Applications in Bioinformatics and Chemistry

17 August 2017

1 reference

17 August 2017

6

1 reference

17 August 2017

29-35

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

17 August 2017

start time

1 June 2013

1 reference

April 2022 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

Consideration of plausible genetic architectures for schizophrenia and implications for analytic approaches in the era of next generation sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

A simple method for assessing the strength of evidence for association at the level of the whole gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

GATES: a rapid and powerful gene-based association test using extended Simes procedure

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

A groupwise association test for rare mutations using a weighted sum statistic

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3685401

25 November 2018

Identifiers

DOI

10.2147/AABC.S44332

1 reference

17 August 2017

1 reference

PMC publication ID

3685401

17 August 2017

PubMed publication ID

23807854

1 reference

PMC publication ID

3685401