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SNP Annotation Toolsnp-nexus.orgCADD - Combined Annotation Dependent Depletion fitCons - Fitness Consequences of Functional Annotation EIGEN - Unsupervised Spectral …

CADD - Combined Annotation Dependent Depletion fitCons - Fitness Consequences of Functional Annotation EIGEN - Unsupervised Spectral …
snp-nexus.org

UCSC Genome Browser Homewww.epigenomebrowser.org/index.html?org=Human&db=hg19&hgsid=11913Welcome to the UCSC Genome Browser website. This site contains the reference sequence and working draft assemblies for a large collection of genomes.

Welcome to the UCSC Genome Browser website. This site contains the reference sequence and working draft assemblies for a large collection of genomes.
www.epigenomebrowser.org/index.html?org=Human&...

http://www.ensembl.org/Homo_sapiens/Info/Indexwww.ensembl.org/Homo_sapiens/Info/IndexWe would like to show you a description here but the site won’t allow us.

We would like to show you a description here but the site won’t allow us.
www.ensembl.org/Homo_sapiens/Info/Index

Human BLAT Searchgenome.ucsc.edu/cgi-bin/hgBlatBLAT on DNA is designed to quickly find sequences of 95% and greater similarity of length 25 bases or more. It may miss more divergent or shorter sequence alignments.

BLAT on DNA is designed to quickly find sequences of 95% and greater similarity of length 25 bases or more. It may miss more divergent or shorter sequence alignments.
genome.ucsc.edu/cgi-bin/hgBlat

Lift Genome Annotationsgenome.ucsc.edu/cgi-bin/hgLiftOverTo lift genome annotations locally on Linux systems, download the liftOver executable and the appropriate chain file.Run liftOver with no arguments to see the usage message.liftOver with no arguments to see the usage message.

To lift genome annotations locally on Linux systems, download the liftOver executable and the appropriate chain file.Run liftOver with no arguments to see the usage message.liftOver with no arguments to see the usage message.
genome.ucsc.edu/cgi-bin/hgLiftOver

GENCODE - Home pagehttps://www.gencodegenes.orgThe GENCODE project produces high quality reference gene annotation and experimental validation for human and mouse genomes

The GENCODE project produces high quality reference gene annotation and experimental validation for human and mouse genomes
www.gencodegenes.org

Reference genome - Wikipediahttps://en.wikipedia.org/wiki/Reference_genomeA reference genome (also known as a reference assembly) is a digital nucleic acid sequence database, assembled by scientists as a representative example of a species' set of genes.As they are often assembled from the sequencing of DNA from a number of donors, reference genomes do not accurately represent the set of genes of any single …

A reference genome (also known as a reference assembly) is a digital nucleic acid sequence database, assembled by scientists as a representative example of a species' set of genes.As they are often assembled from the sequencing of DNA from a number of donors, reference genomes do not accurately represent the set of genes of any single …
en.wikipedia.org/wiki/Reference_genome

Lactose Intolerance: The genetics of not producing …www.geneticlifehacks.com/lactose-intoleranceGlad you are able to figure out the difference here. Actually, the different reference genome (GRCh37 vs. GRCh38) isn’t what causes the allele to need to be flipped here.

Glad you are able to figure out the difference here. Actually, the different reference genome (GRCh37 vs. GRCh38) isn’t what causes the allele to need to be flipped here.
www.geneticlifehacks.com/lactose-intolerance

Sequencing Initiative Suomi (SISu)www.sisuproject.fiThe Sequencing Initiative Suomi (SISu) search engine offers a way to search for data on sequence variants in Finns. It provides valuable summary data for researchers and clinicians as well as other people having an interest in genetics in Finland.

The Sequencing Initiative Suomi (SISu) search engine offers a way to search for data on sequence variants in Finns. It provides valuable summary data for researchers and clinicians as well as other people having an interest in genetics in Finland.
www.sisuproject.fi

Locus Reference Genomic – LRG sequences provide a …www.lrg-sequence.orgLRG sequences provide a stable genomic DNA framework for reporting variants with a permanent ID and core content that never changes.

LRG sequences provide a stable genomic DNA framework for reporting variants with a permanent ID and core content that never changes.
www.lrg-sequence.org