The Alzheimer Disease Sequencing Project (ADSP) Family Based Study The ADSP has
generated whole genome sequence (WGS) data from members of families multiply affected by late onset Alzheimer's disease (LOAD).
Not exact matches
Since 2010
whole genome sequences have been
generated for four Neandertals from Croatia, Siberia and the Russian Caucasus.
To
generate whole -
genome and individual gene nucleotide phylogeny trees, all 95 fully
sequenced unique adenovirus
genomes were first downloaded from GenBank.
Dr. Shendure: Of course the future of genetics includes
sequencing millions or perhaps billions of
whole genomes but I ll be disappointed if
generating and sifting through that data is all our field is capable of.
The Alzheimer's Disease
Sequence Project (ADSP) group is analyzing whole genome and whole exome sequence data generated from samples relevant to Alzheimer's
Sequence Project (ADSP) group is analyzing
whole genome and
whole exome
sequence data generated from samples relevant to Alzheimer's
sequence data
generated from samples relevant to Alzheimer's disease.
We have
generated rich genomic datasets for the scientific community, including an expansive atlas of genetic associations with metabolites,
whole -
genome sequence and phenotype data for population cohorts in the UK10K project, as well as bioinformatic resources to facilitate the retrieval of information, including a metabolite network, a database of genotype - metabolite associations with our colleagues at the HelmHoltz institute, and a
genome browser of UK10K association results.
Complete Genomics provides free public access to a variety of
whole human
genome data sets
generated from Complete Genomics»
sequencing service.
Whole - genome sequencing generates the order of all three billion chemical components in a genome, while whole - exome sequencing targets the 1 to 2 percent of a person's genome that codes for prot
Whole -
genome sequencing generates the order of all three billion chemical components in a
genome, while
whole - exome sequencing targets the 1 to 2 percent of a person's genome that codes for prot
whole - exome
sequencing targets the 1 to 2 percent of a person's
genome that codes for proteins.
Under Dr. Mullikin's leadership, NISC has begun to apply
genome sequencing technologies to clinical research, especially with its largest project, called ClinSeq, for which NISC has
generated more than 500
whole - exome
sequences to date.
The findings of this study will provide valuable insight about how best to present information
generated by
whole genome sequencing to optimize patient care and minimize the unnecessary use of limited healthcare resources.
The list of organisms that have been totally or partially
sequenced continues to grow: As of April 2013,
whole genome sequences have been
generated for 112 vertebrates, along with 455 non-vertebrates and nearly 9,000, mostly harmful, bacteria.
Here, we perform a comprehensive investigation using 3,059 newly
generated low - depth
whole -
genome sequences from eight European isolates and two matched general populations, together with published data from the 1000
Genomes Project and UK10K.
The objective of this project is to leverage ongoing human patient exome and
whole genome sequencing efforts to
generate precision models...
While principal component analysis can reveal relatively old population structure, such as
generated from long - term isolation - by - distance models15,
whole -
genome sequences let us study rare variants to gain insight into more recent population structure.
We
generated the complete
sequence of the
genome by the
whole genome shotgun method, and analysed it with a combination of automatic and manual bioinformatic techniques.
We also
generated a large set of
sequence data including the
whole transcriptomes of ~ 100 species as well as a couple of
genomes.
October 1, 2014 PRA Research Update The University of Missouri has used support from the TTHWF to
generate separate
whole genome sequences from two different Tibetan Terriers with PRA, one with a relatively early onset and the other with a later onset.
I mainly work on data
generated by
whole genome sequencing, whole exome sequencing, targeted resequencing, RNA - seq and Nanopore Sequencing usi
sequencing,
whole exome
sequencing, targeted resequencing, RNA - seq and Nanopore Sequencing usi
sequencing, targeted resequencing, RNA - seq and Nanopore
Sequencing usi
Sequencing using MinION.