An EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype data Anthony YC Kuk1, Xiang Li1 * and Jinfeng Xu2 Background: Pooling is a cost effective way to collect data for genetic association studies, particularly for rare genetic variants. It is of interest to estimate the haplotype frequencies, which contain more information than single locus statistics. By viewing the pooled genotype data as incomplete data, the expectation-maximization (EM) algorithm is the natural algorithm to use, but it is computationally intensive. A recent proposal to reduce the computational burden is to make use of database information to form a list of frequently occurring haplotypes, and to restrict t...
Background: Performing high throughput sequencing on samples pooled from different individuals is a ...
Summary: Genotype calling from high throughput platforms such as Illumina and Affymetrix is a critic...
Thesis (Ph.D.)--University of Washington, 2013Recent emergence of the common disease-rare variant hy...
Background Pooling is a cost effective way to collect data for genetic association studies, particul...
M3-S: a genotype calling method incorporating information from samples with known genotypes Gengxin ...
Background: Along with the improvement of high throughput sequencing technologies, the genetics comm...
Haplotype information could lead to more powerful tests of genetic association than single‐locus ana...
Maximum-parsimony haplotype frequencies inference based on a joint constrained sparse representation...
Motivation: Pooling large number of DNA samples is a common practice in association study, especiall...
Motivation: Information about haplotype structures gives a more detailed picture of genetic variatio...
Background: We address the task of extracting accurate haplotypes from genotype data of individuals ...
Contains fulltext : 34702.pdf (author's version ) (Open Access)We present CVMHAPLO...
Reduced representation sequencing methods such as genotyping-by-sequencing (GBS) enable low-cost mea...
Motivation: It has been claimed in the literature that pooling DNA samples is efficient in estimatin...
Motivation: Pooling large number of DNA samples is a common practice in association study, especiall...
Background: Performing high throughput sequencing on samples pooled from different individuals is a ...
Summary: Genotype calling from high throughput platforms such as Illumina and Affymetrix is a critic...
Thesis (Ph.D.)--University of Washington, 2013Recent emergence of the common disease-rare variant hy...
Background Pooling is a cost effective way to collect data for genetic association studies, particul...
M3-S: a genotype calling method incorporating information from samples with known genotypes Gengxin ...
Background: Along with the improvement of high throughput sequencing technologies, the genetics comm...
Haplotype information could lead to more powerful tests of genetic association than single‐locus ana...
Maximum-parsimony haplotype frequencies inference based on a joint constrained sparse representation...
Motivation: Pooling large number of DNA samples is a common practice in association study, especiall...
Motivation: Information about haplotype structures gives a more detailed picture of genetic variatio...
Background: We address the task of extracting accurate haplotypes from genotype data of individuals ...
Contains fulltext : 34702.pdf (author's version ) (Open Access)We present CVMHAPLO...
Reduced representation sequencing methods such as genotyping-by-sequencing (GBS) enable low-cost mea...
Motivation: It has been claimed in the literature that pooling DNA samples is efficient in estimatin...
Motivation: Pooling large number of DNA samples is a common practice in association study, especiall...
Background: Performing high throughput sequencing on samples pooled from different individuals is a ...
Summary: Genotype calling from high throughput platforms such as Illumina and Affymetrix is a critic...
Thesis (Ph.D.)--University of Washington, 2013Recent emergence of the common disease-rare variant hy...