<p>With the filter settings for genotype frequency <0.01, effect on protein level (functional filter: missense, nonsense, stop loss, splice site, insertions or deletions), and compound heterozygous yields six variants in three genes. <i>MUC16</i> and <i>NBPR10</i> are both genes from large gene families known for their high variability and detection artifacts due to pseudogenes. The heterozygotes in <i>PIGO</i> remain as the likeliest candidates. The <i>Show</i> icon at the right end of the line links to an expert curated annotation database that indicates that the mutation in <i>PIGO</i> is causing Hyperphosphatasia with mental retardation syndrome and has been published in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.p...
Common genetic variability has failed to explain a large fraction of the heritability of complex dis...
The dispensability of individual genes for viability has interested generations of geneticists. For ...
CONTEXT: Hypophosphatasia (HPP) is a syndrome marked by low serum alkaline phosphatase (AlkP) activi...
The identification of disease-causing mutations in next-generation sequencing (NGS) data requires ef...
The identification of disease-causing mutations in next-generation sequencing (NGS) data requires ef...
Hyperphosphatasia mental retardation (HPMR) syndrome is an autosomal recessive form of mental retard...
Over the course of this project, I demonstrate the utility of a 4-phase analysis pipeline in the con...
Contains fulltext : 88212.pdf (publisher's version ) (Closed access)Hyperphosphata...
Motivation: Next-Generation Sequencing (NGS) and exome-capture technologies are currently revolution...
Next-generation sequencing (NGS) has revolutionized genetics and enabled the accurate identification...
Sequencing projects have identified large numbers of rare stop-gain and frameshift variants in the h...
Next-generation sequencing (NGS) has revolutionized genetics and enabled the accurate identification...
Data generation is rapidly progressing and data interpretation is hardly keeping up. New tools and a...
<p>A) In average around 230 variants pass the filter in CEU exomes and 309 in YRI exomes. B) The pot...
Characterization of genetic variation underlying complex phenotypes is incomplete yet critical to un...
Common genetic variability has failed to explain a large fraction of the heritability of complex dis...
The dispensability of individual genes for viability has interested generations of geneticists. For ...
CONTEXT: Hypophosphatasia (HPP) is a syndrome marked by low serum alkaline phosphatase (AlkP) activi...
The identification of disease-causing mutations in next-generation sequencing (NGS) data requires ef...
The identification of disease-causing mutations in next-generation sequencing (NGS) data requires ef...
Hyperphosphatasia mental retardation (HPMR) syndrome is an autosomal recessive form of mental retard...
Over the course of this project, I demonstrate the utility of a 4-phase analysis pipeline in the con...
Contains fulltext : 88212.pdf (publisher's version ) (Closed access)Hyperphosphata...
Motivation: Next-Generation Sequencing (NGS) and exome-capture technologies are currently revolution...
Next-generation sequencing (NGS) has revolutionized genetics and enabled the accurate identification...
Sequencing projects have identified large numbers of rare stop-gain and frameshift variants in the h...
Next-generation sequencing (NGS) has revolutionized genetics and enabled the accurate identification...
Data generation is rapidly progressing and data interpretation is hardly keeping up. New tools and a...
<p>A) In average around 230 variants pass the filter in CEU exomes and 309 in YRI exomes. B) The pot...
Characterization of genetic variation underlying complex phenotypes is incomplete yet critical to un...
Common genetic variability has failed to explain a large fraction of the heritability of complex dis...
The dispensability of individual genes for viability has interested generations of geneticists. For ...
CONTEXT: Hypophosphatasia (HPP) is a syndrome marked by low serum alkaline phosphatase (AlkP) activi...