Hochschulschrift

Exploiting emerging DNA sequencing technologies to study genomic rearrangements

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: Heidelberg, Universität Heidelberg, Dissertation, 2018

Classification: Biowissenschaften, Biologie

Keyword: Bioinformatics
Genetics
Genomes
Cells
Drosophila melanogaster
genetics
bioinformatics
DNA
sequencing
Genetik
Bioinformatik
DNS

Event: Veröffentlichung

(where): Heidelberg

(who): Universitätsbibliothek Heidelberg

(when): 2018

Creator: Meiers, Sascha

Contributor: Zaugg, Judith B.

DOI: 10.11588/heidok.00024506

URN: urn:nbn:de:bsz:16-heidok-245063

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:03 AM CEST

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Hochschulschrift

Associated

Meiers, Sascha
Zaugg, Judith B.
Universitätsbibliothek Heidelberg

Time of origin

2018

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Hochschulschrift

Exploiting emerging DNA sequencing technologies to study genomic rearrangements

Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases

Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes

Forward genetic screen of human transposase genomic rearrangements

Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing

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Disease-causing gene-flanking genomic rearrangements in HNPCC patients

Resolving complex structural genomic rearrangements using a randomized approach

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Hochschulschrift

Exploiting emerging DNA sequencing technologies to study genomic rearrangements

Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases

Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes

Forward genetic screen of human transposase genomic rearrangements

Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing

Enabling technologies of genomic-scale sequence enrichment for targeted high-throughput sequencing

Disease-causing gene-flanking genomic rearrangements in HNPCC patients

Resolving complex structural genomic rearrangements using a randomized approach

Revealing hidden complexities of genomic rearrangements generated with Cas9

Large genomic rearrangements in the CFTRgene contribute to CBAVD

Resection-dependent canonical non-homologous end-joining induces genomic rearrangements

Exploiting genotyping by sequencing to characterize the genomic structure of the American cranberry through high-density linkage mapping

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Exploiting emerging DNA sequencing technologies to study genomic rearrangements

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Other Objects (12)

Exploiting emerging DNA sequencing technologies to study genomic rearrangements

Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases

Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes

Forward genetic screen of human transposase genomic rearrangements

Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing

Enabling technologies of genomic-scale sequence enrichment for targeted high-throughput sequencing

Disease-causing gene-flanking genomic rearrangements in HNPCC patients

Resolving complex structural genomic rearrangements using a randomized approach

Revealing hidden complexities of genomic rearrangements generated with Cas9

Large genomic rearrangements in the CFTRgene contribute to CBAVD

Resection-dependent canonical non-homologous end-joining induces genomic rearrangements

Exploiting genotyping by sequencing to characterize the genomic structure of the American cranberry through high-density linkage mapping

Exploiting emerging DNA sequencing technologies to study genomic rearrangements

Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases

Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes

Forward genetic screen of human transposase genomic rearrangements

Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing

Enabling technologies of genomic-scale sequence enrichment for targeted high-throughput sequencing

Disease-causing gene-flanking genomic rearrangements in HNPCC patients

Resolving complex structural genomic rearrangements using a randomized approach

Revealing hidden complexities of genomic rearrangements generated with Cas9

Large genomic rearrangements in the CFTRgene contribute to CBAVD

Resection-dependent canonical non-homologous end-joining induces genomic rearrangements

Exploiting genotyping by sequencing to characterize the genomic structure of the American cranberry through high-density linkage mapping

Exploiting emerging DNA sequencing technologies to study genomic rearrangements

Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases

Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes

Forward genetic screen of human transposase genomic rearrangements

Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing

Enabling technologies of genomic-scale sequence enrichment for targeted high-throughput sequencing

Disease-causing gene-flanking genomic rearrangements in HNPCC patients

Resolving complex structural genomic rearrangements using a randomized approach

Revealing hidden complexities of genomic rearrangements generated with Cas9

Large genomic rearrangements in the CFTRgene contribute to CBAVD

Resection-dependent canonical non-homologous end-joining induces genomic rearrangements

Exploiting genotyping by sequencing to characterize the genomic structure of the American cranberry through high-density linkage mapping

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