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2. Exome sequencing - Wikipedia

   en.wikipedia.org/wiki/Exome_sequencing

   Exome sequencing workflow: part 1. Exome sequencing, also known as whole exome sequencing (WES), is a genomic technique for sequencing all of the protein-coding regions of genes in a genome (known as the exome). [1] It consists of two steps: the first step is to select only the subset of DNA that encodes proteins.

3. Personal genomics - Wikipedia

   en.wikipedia.org/wiki/Personal_genomics

   The cost must also take into account personnel costs, data processing costs, legal, communications and other costs. One way to assess this is via commercial offerings. The first such whole diploid genome sequencing (6 billion bp, 3 billion from each parent) was from Knome and their price dropped from $350,000 in 2008 to $99,000 in 2009.

4. Helix (genomics company) - Wikipedia

   en.wikipedia.org/wiki/Helix_(genomics_company)

   Helix uses NGS to sequence a proprietary assay called Exome+, a version of Exome sequencing which according to the company provides 100 times more data than was previously available. [9] Exome+ includes all 22,000 protein-coding genes as well as additional regions known to be of interest. [ 10 ]

5. $1,000 genome - Wikipedia

   en.wikipedia.org/wiki/$1,000_genome

   As the costs of sequencing continued to plummet, in 2008, Illumina announced that it had sequenced an individual genome for $100,000 in reagent costs. Applied Biosystems countered by saying the cost on its platform was $60,000. [17] Pacific Biosciences became the latest entrant in what The New York Times called "a heated race for the '$1,000 ...

6. Veritas Genetics - Wikipedia

   en.wikipedia.org/wiki/Veritas_Genetics

   Veritas Genetics is a personal genomics startup based in Danvers, Massachusetts. [1] According to the company's press release, it was among the first companies to offer whole genome sequencing and interpretation for under $1,000.

7. Exome - Wikipedia

   en.wikipedia.org/wiki/Exome

   Whole-exome sequencing is a recent technology that has led to the discovery of various genetic disorders and increased the rate of diagnoses of patients with rare genetic disorders. Overall, whole-exome sequencing has allowed healthcare providers to diagnose 30–50% of patients who were thought to have rare Mendelian disorders.