Publication date
November 2022
DOIAbstract
Release to associate a doi to the article peer-reviewed and recommended by Peer Community in Genomics https://doi.org/10.24072/pci.genomics.10002
Release to associate a doi to the article peer-reviewed and recommended by Peer Community in Genomics https://doi.org/10.24072/pci.genomics.10002
ir l m ter inc ec im improving the ability to detect genomic variation. Along disorders, including A...
This release was used for the analyses published in the paper 'A novel independence test for somatic...
<p>Pathogenic mutations were identified on the basis of seven annotated databases: PKDB, dbSNP, SnpE...
Mutation extraction tools can be combined for robust recognition of genetic variants in the literatu...
Mutation extraction tools can be combined for robust recognition of genetic variants in the literatu...
that examines the genetic basis for individual variations in response to therapeutics. Pharmacogenet...
nipulation, biochemical and molecular experimentation, and the availability of its full genomic sequ...
Rapid screening for phenotype-genotype associations by linear transformations of genomic segments ca...
n whole-genome sequencing “I suggest herein that the genomics research community replace the term ‘i...
Tagging the current state of it to have a DOI for the WIFL genomic vulnerability paper
What's Changed Citation and doi badge by @MMedzin in https://github.com/MMedzin/clustering-genomic-...
ABSTRACT: DNA sequencing has become a powerful method to discover the genetic basis of disease. Stan...
<p>A list of HIV-related PubMed article identifiers (PMIDs) are retrieved from PubMed. The publishin...
Mutations identified using next generation sequencing as stratified by the European society of medic...
"A recommendation – based on reviews by two anonymous reviewers – of the article: Meguerditchian C, ...
ir l m ter inc ec im improving the ability to detect genomic variation. Along disorders, including A...
This release was used for the analyses published in the paper 'A novel independence test for somatic...
<p>Pathogenic mutations were identified on the basis of seven annotated databases: PKDB, dbSNP, SnpE...
Mutation extraction tools can be combined for robust recognition of genetic variants in the literatu...
Mutation extraction tools can be combined for robust recognition of genetic variants in the literatu...
that examines the genetic basis for individual variations in response to therapeutics. Pharmacogenet...
nipulation, biochemical and molecular experimentation, and the availability of its full genomic sequ...
Rapid screening for phenotype-genotype associations by linear transformations of genomic segments ca...
n whole-genome sequencing “I suggest herein that the genomics research community replace the term ‘i...
Tagging the current state of it to have a DOI for the WIFL genomic vulnerability paper
What's Changed Citation and doi badge by @MMedzin in https://github.com/MMedzin/clustering-genomic-...
ABSTRACT: DNA sequencing has become a powerful method to discover the genetic basis of disease. Stan...
<p>A list of HIV-related PubMed article identifiers (PMIDs) are retrieved from PubMed. The publishin...
Mutations identified using next generation sequencing as stratified by the European society of medic...
"A recommendation – based on reviews by two anonymous reviewers – of the article: Meguerditchian C, ...
ir l m ter inc ec im improving the ability to detect genomic variation. Along disorders, including A...
This release was used for the analyses published in the paper 'A novel independence test for somatic...
<p>Pathogenic mutations were identified on the basis of seven annotated databases: PKDB, dbSNP, SnpE...
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