Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q36495652)
Watch
English
Quantitative trait locus analysis for next-generation sequencing with the functional linear models.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
title
Quantitative trait locus analysis for next-generation sequencing with the functional linear models
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
main subject
quantitative trait locus
1 reference
based on heuristic
inferred from title
author
Yun Zhu
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
author name string
Li Luo
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
Momiao Xiong
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
language of work or name
English
0 references
publication date
1 August 2012
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
volume
49
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
issue
8
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
page(s)
513-524
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
cites work
Epigenome-wide association studies for common human diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Rare-variant association testing for sequencing data with the sequence kernel association test
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Optimum designs for next-generation sequencing to discover rare variants for common complex disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Common functional principal components analysis: a new approach to analyzing human movement data.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Association studies for next-generation sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Testing for an unusual distribution of rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
A new testing strategy to identify rare variants with either risk or protective effect on disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Bayesian analysis of rare variants in genetic association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
An evolutionary framework for association testing in resequencing studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Comprehensive approach to analyzing rare genetic variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Statistical analysis strategies for association studies involving rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Pooled association tests for rare variants in exon-resequencing studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
A data-adaptive sum test for disease association with multiple common or rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Understanding mechanisms underlying human gene expression variation with RNA sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Transcriptome genetics using second generation sequencing in a Caucasian population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Population genetic inference from genomic sequence variation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Sequencing technologies - the next generation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
An evaluation of statistical approaches to rare variant analysis in genetic association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Association tests using kernel-based measures of multi-locus genotype similarity between individuals
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Estimation of allele frequencies from high-coverage genome-sequencing projects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
A groupwise association test for rare mutations using a weighted sum statistic
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Using Wavelet-Based Functional Mixed Models to Characterize Population Heterogeneity in Accelerometer Profiles: A Case Study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Accounting for bias from sequencing error in population genetic estimates
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
Generating samples under a Wright-Fisher neutral model of genetic variation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
30 September 2017
To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
28 June 2018
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
21 September 2018
Comparison of methods and sampling designs to test for association between rare variants and quantitative traits.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
21 September 2018
De novo fragment assembly with short mate-paired reads: Does the read length matter?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
21 September 2018
The distribution of rare alleles.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3532851
retrieved
21 September 2018
Identifiers
DOI
10.1136/JMEDGENET-2012-100798
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
PMC publication ID
3532851
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
PubMed publication ID
22889854
1 reference
stated in
Europe PubMed Central
PMC publication ID
3532851
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22889854%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 February 2020
ResearchGate publication ID
230665422
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit