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DNA read errors (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "DNA read errors" in English language version.

refsWebsite
Global rank English rank
11nih.gov
4th place
4th place
7doi.org
2nd place
2nd place
1homolog.us
low place
low place
1web.archive.org
1st place
1st place
1project-management-knowledge.com
low place
low place

doi.org

  • Brown, Alexander J.; Al-Soodani, Aneesa T.; Saul, Miles; Her, Stephanie; Garcia, Juan C.; Ramsden, Dale A.; Her, Chengtao; Roberts, Steven A. (2018). "High-Throughput Analysis of DNA Break-Induced Chromosome Rearrangements by Amplicon Sequencing". Mechanisms of DNA Recombination and Genome Rearrangements: Intersection between Homologous Recombination, DNA Replication and DNA Repair. Methods in Enzymology. Vol. 601. pp. 111–144. doi:10.1016/bs.mie.2017.11.028. ISBN 978-0-12-813979-0. PMC 9703968. PMID 29523230.
  • Simpson, Jared T.; Wong, Kim; Jackman, Shaun D.; Schein, Jacqueline E.; Jones, Steven J.M.; Birol, İnanç (June 2009). "ABySS: A parallel assembler for short read sequence data". Genome Research. 19 (6): 1117–1123. doi:10.1101/gr.089532.108. PMC 2694472. PMID 19251739.
  • Flicek, Paul; Birney, Ewan (November 2009). "Sense from sequence reads: methods for alignment and assembly". Nature Methods. 6 (S11): S6 – S12. doi:10.1038/nmeth.1376. PMID 19844229.
  • Iqbal, Zamin; Caccamo, Mario; Turner, Isaac; Flicek, Paul; McVean, Gil (February 2012). "De novo assembly and genotyping of variants using colored de Bruijn graphs". Nature Genetics. 44 (2): 226–232. doi:10.1038/ng.1028. PMC 3272472. PMID 22231483.
  • Nijkamp, Jurgen F.; van den Broek, Marcel A.; Geertman, Jan-Maarten A.; Reinders, Marcel J. T.; Daran, Jean-Marc G.; de Ridder, Dick (December 2012). "De novo detection of copy number variation by co-assembly". Bioinformatics. 28 (24): 3195–3202. doi:10.1093/bioinformatics/bts601. PMID 23047563.
  • Mesner, Larry D.; Valsakumar, Veena; Cieślik, Marcin; Pickin, Rebecca; Hamlin, Joyce L.; Bekiranov, Stefan (November 2013). "Bubble-seq analysis of the human genome reveals distinct chromatin-mediated mechanisms for regulating early- and late-firing origins". Genome Research. 23 (11): 1774–1788. doi:10.1101/gr.155218.113. PMC 3814878. PMID 23861383.
  • Shuber, A. P.; Michalowsky, L. A.; Scott Nass, G.; Skoletsky, J.; Hire, L. M.; Kotsopoulos, S. K.; Phipps, M. F.; Barberio, D. M.; Klinger, K. W. (March 1997). "High Throughput Parallel Analysis of Hundreds of Patient Samples for More Than 100 Mutations in Multiple Disease Genes". Human Molecular Genetics. 6 (3): 337–347. doi:10.1093/hmg/6.3.337. PMID 9147636.

homolog.us

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Brown, Alexander J.; Al-Soodani, Aneesa T.; Saul, Miles; Her, Stephanie; Garcia, Juan C.; Ramsden, Dale A.; Her, Chengtao; Roberts, Steven A. (2018). "High-Throughput Analysis of DNA Break-Induced Chromosome Rearrangements by Amplicon Sequencing". Mechanisms of DNA Recombination and Genome Rearrangements: Intersection between Homologous Recombination, DNA Replication and DNA Repair. Methods in Enzymology. Vol. 601. pp. 111–144. doi:10.1016/bs.mie.2017.11.028. ISBN 978-0-12-813979-0. PMC 9703968. PMID 29523230.
  • Simpson, Jared T.; Wong, Kim; Jackman, Shaun D.; Schein, Jacqueline E.; Jones, Steven J.M.; Birol, İnanç (June 2009). "ABySS: A parallel assembler for short read sequence data". Genome Research. 19 (6): 1117–1123. doi:10.1101/gr.089532.108. PMC 2694472. PMID 19251739.
  • Flicek, Paul; Birney, Ewan (November 2009). "Sense from sequence reads: methods for alignment and assembly". Nature Methods. 6 (S11): S6 – S12. doi:10.1038/nmeth.1376. PMID 19844229.
  • Iqbal, Zamin; Caccamo, Mario; Turner, Isaac; Flicek, Paul; McVean, Gil (February 2012). "De novo assembly and genotyping of variants using colored de Bruijn graphs". Nature Genetics. 44 (2): 226–232. doi:10.1038/ng.1028. PMC 3272472. PMID 22231483.
  • Nijkamp, Jurgen F.; van den Broek, Marcel A.; Geertman, Jan-Maarten A.; Reinders, Marcel J. T.; Daran, Jean-Marc G.; de Ridder, Dick (December 2012). "De novo detection of copy number variation by co-assembly". Bioinformatics. 28 (24): 3195–3202. doi:10.1093/bioinformatics/bts601. PMID 23047563.
  • Mesner, Larry D.; Valsakumar, Veena; Cieślik, Marcin; Pickin, Rebecca; Hamlin, Joyce L.; Bekiranov, Stefan (November 2013). "Bubble-seq analysis of the human genome reveals distinct chromatin-mediated mechanisms for regulating early- and late-firing origins". Genome Research. 23 (11): 1774–1788. doi:10.1101/gr.155218.113. PMC 3814878. PMID 23861383.
  • Shuber, A. P.; Michalowsky, L. A.; Scott Nass, G.; Skoletsky, J.; Hire, L. M.; Kotsopoulos, S. K.; Phipps, M. F.; Barberio, D. M.; Klinger, K. W. (March 1997). "High Throughput Parallel Analysis of Hundreds of Patient Samples for More Than 100 Mutations in Multiple Disease Genes". Human Molecular Genetics. 6 (3): 337–347. doi:10.1093/hmg/6.3.337. PMID 9147636.

ncbi.nlm.nih.gov

  • Brown, Alexander J.; Al-Soodani, Aneesa T.; Saul, Miles; Her, Stephanie; Garcia, Juan C.; Ramsden, Dale A.; Her, Chengtao; Roberts, Steven A. (2018). "High-Throughput Analysis of DNA Break-Induced Chromosome Rearrangements by Amplicon Sequencing". Mechanisms of DNA Recombination and Genome Rearrangements: Intersection between Homologous Recombination, DNA Replication and DNA Repair. Methods in Enzymology. Vol. 601. pp. 111–144. doi:10.1016/bs.mie.2017.11.028. ISBN 978-0-12-813979-0. PMC 9703968. PMID 29523230.
  • Simpson, Jared T.; Wong, Kim; Jackman, Shaun D.; Schein, Jacqueline E.; Jones, Steven J.M.; Birol, İnanç (June 2009). "ABySS: A parallel assembler for short read sequence data". Genome Research. 19 (6): 1117–1123. doi:10.1101/gr.089532.108. PMC 2694472. PMID 19251739.
  • Iqbal, Zamin; Caccamo, Mario; Turner, Isaac; Flicek, Paul; McVean, Gil (February 2012). "De novo assembly and genotyping of variants using colored de Bruijn graphs". Nature Genetics. 44 (2): 226–232. doi:10.1038/ng.1028. PMC 3272472. PMID 22231483.
  • Mesner, Larry D.; Valsakumar, Veena; Cieślik, Marcin; Pickin, Rebecca; Hamlin, Joyce L.; Bekiranov, Stefan (November 2013). "Bubble-seq analysis of the human genome reveals distinct chromatin-mediated mechanisms for regulating early- and late-firing origins". Genome Research. 23 (11): 1774–1788. doi:10.1101/gr.155218.113. PMC 3814878. PMID 23861383.

project-management-knowledge.com

web.archive.org