Complete Genomics provides free public access to a variety of
whole human genome data sets generated from Complete Genomics» sequencing service.
Not exact matches
By increasing the speed and accuracy for NGS
data analysis like
whole genome sequencing (WGS), our computing platform makes it easier to discover links between DNA sequence variations and
human disease.»
Moreover,
data collected from
whole -
genome sequencing showed that Ata's molecular composition aligned with that of a
human genome.
The most significant of these was the HiSeq X Ten, a 10 - instrument «factory installation» that enabled the most cost - effective
human whole genome sequencing to date: 18,000
genomes per year at a consumables cost of just over $ 1,000 each (note: this does not include the costs of
data storage, analysis, or the $ 10 million buy - in).
This reference database will form the foundation for a national collaboration to share
human whole genome data for the benefit of all scientists.
: an online resource to google and visualize public
human whole genome expression
data.
SweGen: a
whole -
genome data resource of genetic variability in a cross-section of the Swedish population, European Journal of
Human Genetics advance online publication 23 August 2017; doi: 10.1038 / ejhg.2017.130
We focus on developing computational methods and tools for (a) analyzing large - scale gene expression
data related to
human cancer in search for gene markers and disease sub-categories, (b) identifying regulatory elements such as miRNA precursors and their targets in
whole genomes of plants and mammals, (c) building theoretical models of gene regulatory networks.
The project will sequence and analyse
data of 10,000 new
whole genomes across Europe in the next two years, further advancing the understanding of the
human genome for the entire European population.
An open - source C / C + + library of analytical tools for
human genetic variation
data from
whole - exome and
whole -
genome studies.
Analyzes
whole genome and detailed clinical
data from nearly 300,000 Icelanders Finds several novel variations in the sequence of the
human genome modulating cholesterol levels Five variants are also causally linked to increased risk of coronary artery disease Shows...
REYKJAVIK, Iceland, 20 September 2017 — In a major study published today, researchers at deCODE genetics use
whole -
genome data from 14,000 people from across the population of Iceland, including 1500 sets of parents and children, to provide the most detailed portrait to date of how sequence diversity in
humans is the result of an evolving interaction between sex, age, mutation type and location in the
genome.
A diverse
data set of
whole human genomes are freely available for public use to enhance any genomic study or evaluate Complete Genomics
data results and file formats.