Human-specific insertions and deletions inferred from mammalian genome sequences.
about
Predicting the effects of frameshifting indelsCharacterization and potential functional significance of human-chimpanzee large INDEL variationLineage-specific genomics: Frequent birth and death in the human genome: The human genome contains many lineage-specific elements created by both sequence and functional turnoverFine-scale signatures of molecular evolution reconcile models of indel-associated mutationINDELSCAN: a web server for comparative identification of species-specific and non-species-specific insertion/deletion eventsIdentification and analysis of ancestral hominoid transcriptome inferred from cross-species transcript and processed pseudogene comparisonsAncestral alleles in the human genome based on population sequencing dataUsing high-throughput sequencing transcriptome data for INDEL detection: challenges for cancer drug discovery.DNA indels in coding regions reveal selective constraints on protein evolution in the human lineage.A macaque's-eye view of human insertions and deletions: differences in mechanisms.Comparative kinomics of human and chimpanzee reveal unique kinship and functional diversity generated by new domain combinations.Genome and gene alterations by insertions and deletions in the evolution of human and chimpanzee chromosome 22.Phylogenetic inference under varying proportions of indel-induced alignment gaps.Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.Discovery and application of insertion-deletion (INDEL) polymorphisms for QTL mapping of early life-history traits in Atlantic salmonEvolution of genetic and genomic features unique to the human lineage.Exploring the selective constraint on the sizes of insertions and deletions in 5' untranslated regions in mammalsFunctional complementation between transcriptional methylation regulation and post-transcriptional microRNA regulation in the human genome.A defined zebrafish line for high-throughput genetics and genomics: NHGRI-1Detection and characterization of small insertion and deletion genetic variants in modern layer chicken genomes.DiSNPindel: improved intra-individual SNP and InDel detection in direct amplicon sequencing of a diploidSequence context affects the rate of short insertions and deletions in flies and primates.Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletions.Strong heterogeneity in mutation rate causes misleading hallmarks of natural selection on indel mutations in the human genome.CAPIH: a Web interface for comparative analyses and visualization of host-HIV protein-protein interactions.Whole-genome sequencing of Berkshire (European native pig) provides insights into its origin and domestication.Effects of short indels on protein structure and function in human genomesQuantitative prediction of the effect of genetic variation using hidden Markov modelsSequence shortening in the rodent ancestorScanning for the signatures of positive selection for human-specific insertions and deletions.Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.Deciphering the cause of evolutionary variance within intrinsically disordered regions in human proteins.More single-nucleotide mutations surround small insertions than small deletions in primates.
P2860
Q21184005-5CADD5B0-3C99-42DB-9570-68BBAB32F160Q21198753-76BAC560-911C-4A3F-A872-0B1F0BCFC7EEQ28596126-A0C73417-3AFA-4396-B16E-3B88E742C45EQ28681872-03189F63-4170-4E61-BD58-45745871996FQ28757286-CFD0B346-521C-4049-8055-9D71C708898FQ28757526-A7548A9B-1177-44ED-A41C-786B2B71063FQ30000333-48EB506E-D72F-4316-8DCB-8534B831AA3FQ31038214-40325F11-9037-4759-AB6E-86065DEDEEFEQ33302559-B69FD3F7-7BDF-4BAD-92A4-044AC002E0C5Q33302934-F14246C4-D238-4EBF-87D5-EA70BF05B8D0Q33395493-EFA35725-3B88-401D-865D-1C88852A0677Q33403093-E5B439E4-0424-4EB3-AFCE-7A91DE9DC860Q33495765-F60FF847-82EF-4C75-8040-5B1F2267459EQ33527106-13DCF53D-389C-44D0-8D55-DCA041EA8451Q33538313-B73F2137-B84A-448D-89FF-95CA5534C3B6Q33900428-6369737A-AA26-47A7-9EAD-A371C97BA60DQ33949966-DB9B880A-B4D0-4AC6-A96E-9B1CBEB5DE6BQ34173978-DBE4CAA6-C718-4D5D-A2CC-32D0E2842B5FQ34242890-7D9C0072-2A05-4644-A967-CE247E637734Q35728057-4567E4D4-5AF1-4079-8453-84F7AFAB997EQ35820352-DB8FB731-5BC2-4835-9CD5-7F0E384CAF3BQ36642423-0DC88478-858B-4858-A71D-6776E57F4C4DQ37247028-01C68AD5-D2AA-4FF6-B6FB-18489E1F8E39Q37428432-902C6F31-4FFB-4FD0-AD60-E088BD47CF44Q37434235-F08B649F-C04C-48E1-8986-EE861B6FF3D9Q37700345-432EB5B8-8AA0-46F6-A0DD-0F52EA74A762Q41516577-CFC36B9E-AE16-44C3-AEF0-CF160F271831Q41848430-DD5CC0D0-A5DA-43FD-8BF8-2F81637E88EAQ42620212-D6094EA4-7F1E-4BD6-81FC-675B4FD7466FQ42724422-DC1AB10C-EAD9-4AF6-84DC-2550B81517D0Q46189441-0FEB939B-CF49-42F4-95D5-C47622A63C30Q46607962-2E0845A2-DA44-4467-9E52-9639BBD0F6C5Q53097751-835AB7A0-854D-4C1C-98AC-48529F42350B
P2860
Human-specific insertions and deletions inferred from mammalian genome sequences.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Human-specific insertions and deletions inferred from mammalian genome sequences.
@ast
Human-specific insertions and deletions inferred from mammalian genome sequences.
@en
type
label
Human-specific insertions and deletions inferred from mammalian genome sequences.
@ast
Human-specific insertions and deletions inferred from mammalian genome sequences.
@en
prefLabel
Human-specific insertions and deletions inferred from mammalian genome sequences.
@ast
Human-specific insertions and deletions inferred from mammalian genome sequences.
@en
P2093
P2860
P356
P1433
P1476
Human-specific insertions and deletions inferred from mammalian genome sequences.
@en
P2093
Chueng-Jong Chen
Feng-Chi Chen
Trees-Juen Chuang
P2860
P356
10.1101/GR.5429606
P577
2006-11-09T00:00:00Z