Difference between revisions of "KPGP 00122"
From Opengenome.net
(Created page with "<p>Public Profile ID : KPGP_00122 <br /> Gender : F <br /> Nationality : Korea <br /> Ethnic Group : East Asian <br /> Platform : Illumina,HiSeq2000...") |
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Platform : Illumina,HiSeq2000</p> | Platform : Illumina,HiSeq2000</p> | ||
<p> </p> | <p> </p> | ||
| − | <p> | + | <p><b>Public Profile ID</b> : KPGP_00122<br /> |
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| − | <b>Public Profile ID</b> : KPGP_00122<br /> | ||
<b>Genetic data Download</b><br /> | <b>Genetic data Download</b><br /> | ||
| − | <b>Raw Data</b> | + | <b>Raw Data</b> <a target="_blank" href="ftp://14.63.239.232/TGP2011D0011/rawdata">Raw Data</a><br /> |
| − | <b>Aligned Data</b> | + | <b>Aligned Data</b> <a href="ftp://bioftp.org/BiO/Distribute/Open-KPGP/TGP2011D0011/MAPPING_RESULT/KPGP122_G_110915_HiSeq_EastAsian_Kor_F.merge.bam">Mapping</a><br /> |
| − | <b>Nonsynonymous SNVs</b> | + | <b>Nonsynonymous SNVs</b> <a href="ftp://bioftp.org/BiO/Distribute/Open-KPGP/TGP2011D0011/NS_SNV/KPGP122_G_110915_HiSeq_EastAsian_Kor_F.NSSNV.gz">Nonsynonymous SNVs</a><br /> |
| − | <b>Read me</b> | + | <b>Read me</b> <a target="_blank" href="ftp://bioftp.org/BiO/Distribute/Open-KPGP/TGP2011D0011/README/KPGP_122.readme.txt">Read me</a><br /> |
| − | <b>Genome Variation</b> | + | <b>Genome Variation</b> <a href="ftp://bioftp.org/BiO/Distribute/Open-KPGP/TGP2011D0011/SNV/KPGP122_G_110915_HiSeq_EastAsian_Kor_F.vcf.SNV.gz">SNVs</a> <a href="nofile">CNVs</a> <a href="ftp://bioftp.org/BiO/Distribute/Open-KPGP/TGP2011D0011/INDEL/KPGP122_G_110915_HiSeq_EastAsian_Kor_F.vcf.INDEL.gz">INDELs</a> <a href="ftp://bioftp.org/BiO/Distribute/Open-KPGP/TGP2011D0011/SV/KPGP122_G_110915_HiSeq_EastAsian_Kor_F.sv.gz">SVs</a> <br /> |
| + | </p> | ||
Revision as of 15:08, 8 November 2011
Public Profile ID : KPGP_00122
Gender : F
Nationality : Korea
Ethnic Group : East Asian
Platform : Illumina,HiSeq2000
Public Profile ID : KPGP_00122
Genetic data Download
Raw Data Raw Data
Aligned Data Mapping
Nonsynonymous SNVs Nonsynonymous SNVs
Read me Read me
Genome Variation SNVs CNVs INDELs SVs
