With the increasing number of sequencing projects involving families, quality control tools optimized for family genome sequencing are needed. However, accurately quantifying contamination in a DNA mixture is particularly difficult when genetically related family members are the sources. We developed TrioMix, a maximum likelihood estimation (MLE) framework based on Mendel’s law of inheritance, to quantify DNA mixture between family members in genome sequencing data of parent–offspring trios. TrioMix can accurately deconvolute any intrafamilial DNA contamination, including parent–offspring, sibling–sibling, parent–parent, and even multiple familial sources. In addition, TrioMix can be applied to detect genomic abnormalities that deviate from...
Background: As sequencing technologies can help researchers detect common and rare variants across t...
Sequencing DNA in extended multiplex families can help to identify high penetrance disease variants ...
Next generation sequencing technology has been widely used in genomic analysis, but its application ...
We analyzed the whole genome sequences of a family of four, consisting of two siblings and their par...
Sequencing family DNA samples provides an attractive alternative to population based designs to iden...
Although the technical and analytic complexity of whole genome sequencing is generally appreciated, ...
Sequencing family DNA samples provides an attractive alternative to population based de-signs to ide...
Motivation: A basic problem of broad public and scientific interest is to use the DNA of an individu...
When analyzing family data, we dream of perfectly informative data, even whole-genome sequences (WGS...
We analyzed the whole genome sequences of a family of four, consisting of two siblings and their par...
MOTIVATION: Next generation sequencing (NGS) technology considerably changed the way we screen for p...
Background: As sequencing technologies can help researchers detect common and rare variants across t...
Background: In the course of our whole-genome sequencing efforts, we have developed a pipeline for a...
Summary: TrioVis is a visual analytics tool developed for filtering on coverage and variant frequenc...
Thesis (Ph.D.)--University of Washington, 2013Recent emergence of the common disease-rare variant hy...
Background: As sequencing technologies can help researchers detect common and rare variants across t...
Sequencing DNA in extended multiplex families can help to identify high penetrance disease variants ...
Next generation sequencing technology has been widely used in genomic analysis, but its application ...
We analyzed the whole genome sequences of a family of four, consisting of two siblings and their par...
Sequencing family DNA samples provides an attractive alternative to population based designs to iden...
Although the technical and analytic complexity of whole genome sequencing is generally appreciated, ...
Sequencing family DNA samples provides an attractive alternative to population based de-signs to ide...
Motivation: A basic problem of broad public and scientific interest is to use the DNA of an individu...
When analyzing family data, we dream of perfectly informative data, even whole-genome sequences (WGS...
We analyzed the whole genome sequences of a family of four, consisting of two siblings and their par...
MOTIVATION: Next generation sequencing (NGS) technology considerably changed the way we screen for p...
Background: As sequencing technologies can help researchers detect common and rare variants across t...
Background: In the course of our whole-genome sequencing efforts, we have developed a pipeline for a...
Summary: TrioVis is a visual analytics tool developed for filtering on coverage and variant frequenc...
Thesis (Ph.D.)--University of Washington, 2013Recent emergence of the common disease-rare variant hy...
Background: As sequencing technologies can help researchers detect common and rare variants across t...
Sequencing DNA in extended multiplex families can help to identify high penetrance disease variants ...
Next generation sequencing technology has been widely used in genomic analysis, but its application ...