Read (Portuguese Wikipedia)
Analysis of information sources in references of the Wikipedia article "Read" in Portuguese language version.
refsWebsite
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low place
bredagenetics.com
- «Sequencing library: what is it?». Breda Genetics. 12 de agosto de 2016. Consultado em 23 de julho de 2017
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: 336–346. PMC 2652199
. PMID 19056694. doi:10.1101/gr.079053.108. Consultado em 23 de julho de 2017
doi.org
dx.doi.org
- Chaisson, Mark J. (2009). «De novo fragment assembly with short mate-paired reads: Does the read length matter?». Genome Research. 19: 336–346. PMC 2652199. PMID 19056694. doi:10.1101/gr.079053.108. Consultado em 23 de julho de 2017
- Junemann, Sebastian (2013). «Updating benchtop sequencing performance comparison». Nature Biotechnology. 31: 294–296. PMID 23563421. doi:10.1038/nbt.2522
- 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: 341. PMC 3431227. PMID 22827831. doi:10.1186/1471-2164-13-341
- Chhangawala, Sagar; Rudy, Gabe; Mason, Christopher E.; Rosenfeld, Jeffrey A. (23 de junho de 2015). «The impact of read length on quantification of differentially expressed genes and splice junction detection». Genome Biology. 16. 131 páginas. PMC 4531809. PMID 26100517. doi:10.1186/s13059-015-0697-y
- Chaisson, Mark J.P. (2015). «Genetic variation and the de novo assembly of human genomes». Nature Reviews Genetics. 16: 627–640. PMC 4745987. PMID 26442640. doi:10.1038/nrg3933
- Conesa, Ana; Madrigal, Pedro; Tarazona, Sonia; Gomez-Cabrero, David; Cervera, Alejandra; McPherson, Andrew; Szcześniak, Michał Wojciech; Gaffney, Daniel J.; Elo, Laura L. (26 de janeiro de 2016). «A survey of best practices for RNA-seq data analysis». Genome Biology. 17. 13 páginas. PMC 4728800. PMID 26813401. doi:10.1186/s13059-016-0881-8
nih.gov
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: 336–346. PMC 2652199. PMID 19056694. doi:10.1101/gr.079053.108. Consultado em 23 de julho de 2017
- Junemann, Sebastian (2013). «Updating benchtop sequencing performance comparison». Nature Biotechnology. 31: 294–296. PMID 23563421. doi:10.1038/nbt.2522
- 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: 341. PMC 3431227. PMID 22827831. doi:10.1186/1471-2164-13-341
- Chhangawala, Sagar; Rudy, Gabe; Mason, Christopher E.; Rosenfeld, Jeffrey A. (23 de junho de 2015). «The impact of read length on quantification of differentially expressed genes and splice junction detection». Genome Biology. 16. 131 páginas. PMC 4531809. PMID 26100517. doi:10.1186/s13059-015-0697-y
- Chaisson, Mark J.P. (2015). «Genetic variation and the de novo assembly of human genomes». Nature Reviews Genetics. 16: 627–640. PMC 4745987. PMID 26442640. doi:10.1038/nrg3933
- Conesa, Ana; Madrigal, Pedro; Tarazona, Sonia; Gomez-Cabrero, David; Cervera, Alejandra; McPherson, Andrew; Szcześniak, Michał Wojciech; Gaffney, Daniel J.; Elo, Laura L. (26 de janeiro de 2016). «A survey of best practices for RNA-seq data analysis». Genome Biology. 17. 13 páginas. PMC 4728800. PMID 26813401. doi:10.1186/s13059-016-0881-8