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http://www.nature.com/nature/journal/v456/n7218/edsumm/e081106-01.html
話說這期的Nature還真的是有給他精采到, 第一次有這種頂級學術期刊花了將近半本本來討論這種問題, 會說精彩是因為並不是像以前一樣弄了台千萬儀器就在那邊high了個半死, 而是全面性的從社會角度與醫學角度出發來看這技術,包括個人隱私與健康等等的議題.
ps.
其實裡邊沒仔細看(該死的期中考), 但是看到一張圖似乎是ralationship tree, 有三個字在上邊: Y.H., Venter, Watson ............. orz
仔細想想就知道這是啥 XD
DNA and sequencing
DNA samples (NA07340 and NA18507) and cell line (GM07340) were obtained from Coriell Repositories. DNA samples were genotyped on the HM550 array and the results compared to publicly available data to confirm their identity before use. Methods for DNA manipulation, including sample preparation, formation of single-molecule arrays, cluster growth and sequencing were all developed during this study and formed the basis for the standard protocols now available from Illumina, Inc. All sequencing was performed on Illumina GA1s equipped with a one-megapixel camera. All purity filtered read data are available for download from the Short Read Archive at NCBI or from the European Short Read Archive (ERA) at the EBI.
Analysis software
Image analysis software and the ELAND aligner are provided as part of the Genome Analyzer analysis software. SNP and structural variant detectors will be available as future upgrades of the analysis pipeline. The Resembl extension to Ensembl is available on request. The MAQ (Mapping and Assembly with Qualities) aligner is freely available for download from http://maq.sourceforge.net.
Data access
Sequence data for NA18507 are freely available from the NCBI short read archive, accession SRA000271 (ftp://ftp.ncbi.nih.gov/pub/TraceDB/ShortRead/SRA000271). X chromosome data are freely available from ERA, accession ERA000035. Links to Resembl displays for chromosome X and human data, plus information on other available data, are provided at http://www.illumina.com/HumanGenome.
話說這期的Nature還真的是有給他精采到, 第一次有這種頂級學術期刊花了將近半本本來討論這種問題, 會說精彩是因為並不是像以前一樣弄了台千萬儀器就在那邊high了個半死, 而是全面性的從社會角度與醫學角度出發來看這技術,包括個人隱私與健康等等的議題.
ps.
其實裡邊沒仔細看(該死的期中考), 但是看到一張圖似乎是ralationship tree, 有三個字在上邊: Y.H., Venter, Watson ............. orz
仔細想想就知道這是啥 XD
DNA and sequencing
DNA samples (NA07340 and NA18507) and cell line (GM07340) were obtained from Coriell Repositories. DNA samples were genotyped on the HM550 array and the results compared to publicly available data to confirm their identity before use. Methods for DNA manipulation, including sample preparation, formation of single-molecule arrays, cluster growth and sequencing were all developed during this study and formed the basis for the standard protocols now available from Illumina, Inc. All sequencing was performed on Illumina GA1s equipped with a one-megapixel camera. All purity filtered read data are available for download from the Short Read Archive at NCBI or from the European Short Read Archive (ERA) at the EBI.
Analysis software
Image analysis software and the ELAND aligner are provided as part of the Genome Analyzer analysis software. SNP and structural variant detectors will be available as future upgrades of the analysis pipeline. The Resembl extension to Ensembl is available on request. The MAQ (Mapping and Assembly with Qualities) aligner is freely available for download from http://maq.sourceforge.net.
Data access
Sequence data for NA18507 are freely available from the NCBI short read archive, accession SRA000271 (ftp://ftp.ncbi.nih.gov/pub/TraceDB/ShortRead/SRA000271). X chromosome data are freely available from ERA, accession ERA000035. Links to Resembl displays for chromosome X and human data, plus information on other available data, are provided at http://www.illumina.com/HumanGenome.
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