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Anish Kejariwal

Researcher at Celera Corporation

Publications -  14
Citations -  20649

Anish Kejariwal is an academic researcher from Celera Corporation. The author has contributed to research in topics: Genome & Gene density. The author has an hindex of 14, co-authored 14 publications receiving 19707 citations. Previous affiliations of Anish Kejariwal include Applied Biosystems & SRI International.

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Journal ArticleDOI

The sequence of the human genome.

J. Craig Venter, +272 more
- 16 Feb 2001 - 
TL;DR: Comparative genomic analysis indicates vertebrate expansions of genes associated with neuronal function, with tissue-specific developmental regulation, and with the hemostasis and immune systems are indicated.
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PANTHER: a library of protein families and subfamilies indexed by function.

TL;DR: The PANTHER/X ontology is used to give a high-level representation of gene function across the human and mouse genomes, and the family HMMs are used to rank missense single nucleotide polymorphisms (SNPs) according to their likelihood of affecting protein function.
Journal ArticleDOI

The Sequence of the Human Genome

J. Craig Venter, +272 more
- 01 Sep 2015 - 
TL;DR: Comparative genomic analysis indicates vertebrate expansions of genes associated with neuronal function, with tissue-specific developmental regulation, and with the hemostasis and immune systems are indicated.
Journal ArticleDOI

The PANTHER database of protein families, subfamilies, functions and pathways.

TL;DR: PANTHER is a large collection of protein families that have been subdivided into functionally related subfamilies, using human expertise, allowing more accurate association with function, as well as inference of amino acids important for functional specificity.
Journal ArticleDOI

Inferring Nonneutral Evolution from Human-Chimp-Mouse Orthologous Gene Trios

TL;DR: Partitions of genes into inferred biological classes identified accelerated evolution in several functional classes, including olfaction and nuclear transport and human-accelerated genes are significantly more likely to underlie major known Mendelian disorders.