リード (生物学) (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "リード (生物学)" in Japanese language version.

refsWebsite

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1bredagenetics.com

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bredagenetics.com

“Sequencing library: what is it?”. Breda Genetics (2016年8月12日). 2017年7月23日閲覧。

cshlp.org

genome.cshlp.org

Chaisson, Mark J. (2009). “De novo fragment assembly with short mate-paired reads: Does the read length matter?”. Genome Research 19 (2): 336–346. doi:10.1101/gr.079053.108. PMC 2652199. PMID 19056694 2017年7月23日閲覧。.

doi.org

Chaisson, Mark J. (2009). “De novo fragment assembly with short mate-paired reads: Does the read length matter?”. Genome Research 19 (2): 336–346. doi:10.1101/gr.079053.108. PMC 2652199. PMID 19056694 2017年7月23日閲覧。.
Junemann, Sebastian (2013). “Updating benchtop sequencing performance comparison”. Nature Biotechnology 31 (4): 294–296. doi:10.1038/nbt.2522. PMID 23563421.
Quail, Michael A. (2012). “A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers”. BMC Genomics 13 (1): 341. doi:10.1186/1471-2164-13-341. PMC 3431227. PMID 22827831.
Chhangawala, Sagar; Rudy, Gabe; Mason, Christopher E.; Rosenfeld, Jeffrey A. (23 June 2015). “The impact of read length on quantification of differentially expressed genes and splice junction detection”. Genome Biology 16 (1): 131. doi:10.1186/s13059-015-0697-y. PMC 4531809. PMID 26100517.
Chaisson, Mark J.P. (2015). “Genetic variation and the de novo assembly of human genomes”. Nature Reviews Genetics 16 (11): 627–640. doi:10.1038/nrg3933. PMC 4745987. PMID 26442640.
Conesa, Ana; Madrigal, Pedro; Tarazona, Sonia; Gomez-Cabrero, David; Cervera, Alejandra; McPherson, Andrew; Szcześniak, Michał Wojciech; Gaffney, Daniel J. et al. (26 January 2016). “A survey of best practices for RNA-seq data analysis”. Genome Biology 17 (1): 13. doi:10.1186/s13059-016-0881-8. PMC 4728800. PMID 26813401.

nih.gov

pubmed.ncbi.nlm.nih.gov

Chaisson, Mark J. (2009). “De novo fragment assembly with short mate-paired reads: Does the read length matter?”. Genome Research 19 (2): 336–346. doi:10.1101/gr.079053.108. PMC 2652199. PMID 19056694 2017年7月23日閲覧。.
Junemann, Sebastian (2013). “Updating benchtop sequencing performance comparison”. Nature Biotechnology 31 (4): 294–296. doi:10.1038/nbt.2522. PMID 23563421.
Quail, Michael A. (2012). “A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers”. BMC Genomics 13 (1): 341. doi:10.1186/1471-2164-13-341. PMC 3431227. PMID 22827831.
Chhangawala, Sagar; Rudy, Gabe; Mason, Christopher E.; Rosenfeld, Jeffrey A. (23 June 2015). “The impact of read length on quantification of differentially expressed genes and splice junction detection”. Genome Biology 16 (1): 131. doi:10.1186/s13059-015-0697-y. PMC 4531809. PMID 26100517.
Chaisson, Mark J.P. (2015). “Genetic variation and the de novo assembly of human genomes”. Nature Reviews Genetics 16 (11): 627–640. doi:10.1038/nrg3933. PMC 4745987. PMID 26442640.
Conesa, Ana; Madrigal, Pedro; Tarazona, Sonia; Gomez-Cabrero, David; Cervera, Alejandra; McPherson, Andrew; Szcześniak, Michał Wojciech; Gaffney, Daniel J. et al. (26 January 2016). “A survey of best practices for RNA-seq data analysis”. Genome Biology 17 (1): 13. doi:10.1186/s13059-016-0881-8. PMC 4728800. PMID 26813401.

pmc.ncbi.nlm.nih.gov

Chaisson, Mark J. (2009). “De novo fragment assembly with short mate-paired reads: Does the read length matter?”. Genome Research 19 (2): 336–346. doi:10.1101/gr.079053.108. PMC 2652199. PMID 19056694 2017年7月23日閲覧。.
Quail, Michael A. (2012). “A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers”. BMC Genomics 13 (1): 341. doi:10.1186/1471-2164-13-341. PMC 3431227. PMID 22827831.
Chhangawala, Sagar; Rudy, Gabe; Mason, Christopher E.; Rosenfeld, Jeffrey A. (23 June 2015). “The impact of read length on quantification of differentially expressed genes and splice junction detection”. Genome Biology 16 (1): 131. doi:10.1186/s13059-015-0697-y. PMC 4531809. PMID 26100517.
Chaisson, Mark J.P. (2015). “Genetic variation and the de novo assembly of human genomes”. Nature Reviews Genetics 16 (11): 627–640. doi:10.1038/nrg3933. PMC 4745987. PMID 26442640.
Conesa, Ana; Madrigal, Pedro; Tarazona, Sonia; Gomez-Cabrero, David; Cervera, Alejandra; McPherson, Andrew; Szcześniak, Michał Wojciech; Gaffney, Daniel J. et al. (26 January 2016). “A survey of best practices for RNA-seq data analysis”. Genome Biology 17 (1): 13. doi:10.1186/s13059-016-0881-8. PMC 4728800. PMID 26813401.

ncbi.nlm.nih.gov

Quail, Michael A. (2012). “A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers”. BMC Genomics 13 (1): 341. doi:10.1186/1471-2164-13-341. PMC 3431227. PMID 22827831.
Chhangawala, Sagar; Rudy, Gabe; Mason, Christopher E.; Rosenfeld, Jeffrey A. (23 June 2015). “The impact of read length on quantification of differentially expressed genes and splice junction detection”. Genome Biology 16 (1): 131. doi:10.1186/s13059-015-0697-y. PMC 4531809. PMID 26100517.
Chaisson, Mark J.P. (2015). “Genetic variation and the de novo assembly of human genomes”. Nature Reviews Genetics 16 (11): 627–640. doi:10.1038/nrg3933. PMC 4745987. PMID 26442640.
Conesa, Ana; Madrigal, Pedro; Tarazona, Sonia; Gomez-Cabrero, David; Cervera, Alejandra; McPherson, Andrew; Szcześniak, Michał Wojciech; Gaffney, Daniel J. et al. (26 January 2016). “A survey of best practices for RNA-seq data analysis”. Genome Biology 17 (1): 13. doi:10.1186/s13059-016-0881-8. PMC 4728800. PMID 26813401.