Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition - Wikidata - wikimedia - TriplyDB

Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

http://www.wikidata.org/entity/Q28776447

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Hot L1s account for the bulk of retrotransposition in the human population Whole-genome experimental identification of insertion/deletion polymorphisms of interspersed repeats by a new general approach Roles for retrotransposon insertions in human disease The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes Human transposon tectonics Detection of Cytosine methylation in ancient DNA from five native american populations using bisulfite sequencing LINE-1 elements in structural variation and disease LINE-1 retrotransposition activity in human genomes High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes Microarray-based global mapping of integration sites for the retrotransposon, intracisternal A-particle, in the mouse genome dbRIP: a highly integrated database of retrotransposon insertion polymorphisms in humans Different evolutionary fates of recently integrated human and chimpanzee LINE-1 retrotransposons Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion Natural mutagenesis of human genomes by endogenous retrotransposons Genome-wide comparison of differences in the integration sites of interspersed repeats between closely related genomes.The Role of Somatic L1 Retrotransposition in Human Cancers.The protist Trichomonas vaginalis harbors multiple lineages of transcriptionally active Mutator-like elements Mobile element scanning (ME-Scan) by targeted high-throughput sequencing.Copy number variations in East-Asian population and their evolutionary and functional implications RISCI--Repeat Induced Sequence Changes Identifier: a comprehensive, comparative genomics-based, in silico subtractive hybridization pipeline to identify repeat induced sequence changes in closely related genomes Hypomethylation of intragenic LINE-1 represses transcription in cancer cells through AGO2.Large differences between LINE-1 amplification rates in the human and chimpanzee lineages.ATLAS: a system to selectively identify human-specific L1 insertions.Allelic heterogeneity in LINE-1 retrotransposition activity.SVA elements are nonautonomous retrotransposons that cause disease in humans.Reading TE leaves: new approaches to the identification of transposable element insertions.Mobilizing diversity: transposable element insertions in genetic variation and disease.De novo LINE-1 retrotransposition in HepG2 cells preferentially targets gene poor regions of chromosome 13 Abundant raw material for cis-regulatory evolution in humans.Association of an allele on chromosome 9 and abdominal aortic aneurysm.Effects of L1-ORF2 fragments on green fluorescent protein gene expression Natural genetic variation caused by transposable elements in humans Human endogenous retroviral elements as indicators of ectopic recombination events in the primate genome.Extensive individual variation in L1 retrotransposition capability contributes to human genetic diversity Mobile element scanning (ME-Scan) identifies thousands of novel Alu insertions in diverse human populations.Dynamic interactions between transposable elements and their hosts.The insertional history of an active family of L1 retrotransposons in humans Active Alu element "A-tails": size does matter The recent evolution of human L1 retrotransposons.Genome-wide experimental identification and functional analysis of human specific retroelements.

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

http://www.wikidata.org/entity/Q28776447

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2000 nî lūn-bûn

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2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2000 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition

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F M Sheen

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P2860

The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data.

Genetic traces of ancient demography

Genomic sequencing

Basic local alignment search tool

A recent insertion of an alu element on the Y chromosome is a useful marker for human population studies

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

Using mitochondrial and nuclear DNA markers to reconstruct human evolution

Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa

High resolution of human evolutionary trees with polymorphic microsatellites

Origin and evolution of retroelements based upon their reverse transcriptase sequences

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10.1101/GR.149400

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