(Q37940824)

25 August 2017

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title

Challenges in studying genomic structural variant formation mechanisms: the short-read dilemma and beyond (English)

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25 August 2017

2

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25 August 2017

Megumi Onishi-Seebacher

series ordinal

1

object named as

Megumi Onishi-Seebacher

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25 August 2017

language of work or name

English

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publication date

30 September 2011

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25 August 2017

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25 August 2017

volume

33

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25 August 2017

issue

11

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25 August 2017

page(s)

840-850

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Mapping copy number variation by population-scale genome sequencing

25 August 2017

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Nuclear receptor-induced chromosomal proximity and DNA breaks underlie specific translocations in cancer

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Regulation of homologous recombination in eukaryotes

21 January 2018

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The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway

21 January 2018

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MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings

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Synthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions

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21 January 2018

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21 January 2018

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Genome structural variation discovery and genotyping

21 January 2018

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Fine-scale structural variation of the human genome

21 January 2018

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Mapping and sequencing of structural variation from eight human genomes

21 January 2018

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Why repetitive DNA is essential to genome function

21 January 2018

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Repeat instability as the basis for human diseases and as a potential target for therapy

21 January 2018

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Mechanisms for human genomic rearrangements

21 January 2018

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Genetic and epigenetic mechanisms underlying cell-surface variability in protozoa and fungi

21 January 2018

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High-resolution copy-number variation map reflects human olfactory receptor diversity and evolution

21 January 2018

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LINE-1 retrotransposons: mediators of somatic variation in neuronal genomes?

21 January 2018

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Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes

21 January 2018

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Finishing the euchromatic sequence of the human genome

21 January 2018

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Characterization of missing human genome sequences and copy-number polymorphic insertions

21 January 2018

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Amplification-free Illumina sequencing-library preparation facilitates improved mapping and assembly of (G+C)-biased genomes

21 January 2018

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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries

21 January 2018

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Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

21 January 2018

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Mobile interspersed repeats are major structural variants in the human genome

21 January 2018

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Natural mutagenesis of human genomes by endogenous retrotransposons

21 January 2018

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LINE-1 retrotransposition activity in human genomes

21 January 2018

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High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes

21 January 2018

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De novo assembly of human genomes with massively parallel short read sequencing

21 January 2018

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Company profile: Complete Genomics Inc.

21 January 2018

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DNA transposon Hermes inserts into DNA in nucleosome-free regions in vivo

21 January 2018

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The genomic complexity of primary human prostate cancer

21 January 2018

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Transcriptional repression mediated by repositioning of genes to the nuclear lamina

21 January 2018

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Molecular maps of the reorganization of genome-nuclear lamina interactions during differentiation

21 January 2018

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The nuclear envelope in genome organization, expression and stability

21 January 2018

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Cohesin: its roles and mechanisms

21 January 2018

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One-hit wonders of genomic instability.

21 January 2018

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Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers

21 January 2018

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The expanding universe of cohesin functions: a new genome stability caretaker involved in human disease and cancer.

21 January 2018

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Breakpoints of gross deletions coincide with non-B DNA conformations

21 January 2018

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Non-B DNA structure-induced genetic instability

21 January 2018

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Non-B DNA structure-induced genetic instability and evolution

21 January 2018

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DNA structures at chromosomal translocation sites

21 January 2018

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Non-B DNA conformations as determinants of mutagenesis and human disease

21 January 2018

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Genome-wide analyses of recombination prone regions predict role of DNA structural motif in recombination

21 January 2018

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Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

21 January 2018

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Genome-wide analysis reveals novel molecular features of mouse recombination hotspots

21 January 2018

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https://api.crossref.org/works/10.1002%2FBIES.201100075

Long-range oncogenic activation of Igh-c-myc translocations by the Igh 3' regulatory region.

21 January 2018

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Mechanisms promoting translocations in editing and switching peripheral B cells

21 January 2018

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Comprehensive mapping of long-range interactions reveals folding principles of the human genome

21 January 2018

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Evolutionary footprints of nucleosome positions in yeast

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/BIES.201100075

1 reference

release_e2dkuvlcyvca7lxkyrfa6ohbpa

25 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/e2dkuvlcyvca7lxkyrfa6ohbpa

mapped directly with Wikidata item

24 November 2022

based on heuristic

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