- The
Single Nucleotide Polymorphism Database (
dbSNP) is a free
public archive for
genetic variation within and
across different species developed and hosted...
-
United States National Library of Medicine. 2014. NCBI
dbSNP build 142 for human. "[
DBSNP-announce]
DBSNP Human Build 142 (GRCh38 and GRCh37.p13)". Archived...
-
mutation at
position 342 (
dbSNP: rs28929474),
while PiS is
caused by a
glutamic acid to
valine mutation at
position 264 (
dbSNP: rs17580).
Other rarer forms...
-
known as
genomic selection. Crop-specific
arrays find use in agriculture. "
dbSNP Summary". www.ncbi.nlm.nih.gov.
Retrieved 4
October 2017. The 1000 Genomes...
-
annotation (
SNP annotation) is the
process of
predicting the
effect or
function of an
individual SNP using SNP annotation tools. In
SNP annotation the...
- (
SNPs) in
public databases such as
dbSNP. More
common recessive phenotypes would be more
likely to have disease-causing
variants reported in
dbSNP. For...
-
annotation tracks,
including gene predictions, mRNA/EST alignments, and
SNP markers, all
presented in a
scrollable view.
Users could also add custom...
- PMID 23824865.{{cite book}}: CS1 maint:
location missing publisher (link) "
DBSNP Home Page".
National Center for
Biotechnology Information, U.S. National...
- are do****ented in
specific databases. The
variants could be
obtained from
dbSNP, 1000
Genomes Project, or user-supplied list.
Additional information could...
- po****tion. 1.
Introduce the
reference of a
SNP of interest, as an example: rs429358, in a
database (
dbSNP or other). 2. Find MAF/MinorAlleleCount link...
