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Genomics / DNA sequencing / DNA / Bioinformatics / Full genome sequencing / Exome sequencing / Expressed sequence tag / Single-nucleotide polymorphism / 454 Life Sciences / Biology / Genetics / Molecular biology


guest editorial GuestEditorial BY MEGAN GROVE, MS, CGC, GENETIC COUNSELOR, STANFORD CLINICAL GENOMICS SERVICE AND STANFORD CENTER FOR INHERITED CARDIOVASCULAR DISEASE
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Document Date: 2014-06-25 19:38:04

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File Size: 52,01 KB

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Facility

Lucile Packard Children’s Hospital / Stanford Hospital / Stanford University / /

IndustryTerm

variant calling algorithms / bioinformatics algorithms / computational tools / /

MedicalCondition

rare and undiagnosed genetic diseases / undiagnosed diseases / mendelian disorders / disease / appropriate cancer / important inherited disease / severe childhood recessive diseases / MS / genetic diseases / given tumor / /

Organization

Lucile Packard Children’s Hospital / Stanford University / NIH National Center / Stanford Hospital / STANFORD CLINICAL GENOMICS SERVICE AND STANFORD CENTER FOR INHERITED CARDIOVASCULAR DISEASE Genomic Sequencing / /

Person

Rachel Goldfeder / MEGAN GROVE / Euan Ashley / /

Position

author / /

SportsLeague

Stanford University / /

Technology

variant calling algorithms / Simulation / bioinformatics algorithms / CLINICAL GENOMICS / /

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