Result for 5C518D01E5610BDDC5A207514542E4D38D16E5D6

Query result

Key Value
FileName./usr/lib64/R/library/Rsolid/html/00Index.html
FileSize1185
MD595D420157B948958A0E9919A103C3D39
SHA-15C518D01E5610BDDC5A207514542E4D38D16E5D6
SHA-25635764C9076BB0C24E523B4DBADD87280A334A8468F7AA88111B1FA71CF89438F
SSDEEP24:hMTIXF0SspbTXF0PPpM26MFvujMR0F4h/1YZp5dLyNtiXF2g:BepbT4hMMQ4eVLIti8g
TLSHT131216736E0643B177823995186C02ED857616622770A9E4D2F0D347B42093EF22337AE
hashlookup:parent-total31
hashlookup:trust100

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Parents (Total: 31)

The searched file hash is included in 31 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
MD50E6C6EF234DEFCD727BB7B91EE2A26A7
PackageArchs390x
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease14.fc22
PackageVersion0.9.31
SHA-1071A0ABEC65452F78DB94941A4E6763983BA4212
SHA-25674A907FD50D102B29FD977AA9BE90800D90F290C71A7B2A7FFD6C1059024E914
Key Value
MD56DC22CB598E860FA9F159C434D45B689
PackageArchppc64le
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease13.fc21
PackageVersion0.9.31
SHA-1208B109F863FE29FCC56C9AB1004CD62E3858274
SHA-256E2A04407071D32F39AB8E02702AC1C207301C69460C15C43742AD909F524D22B
Key Value
MD577EEFBAB8B025020DDFB7E8A33FE2508
PackageArchppc64
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease9.fc19
PackageVersion0.9.31
SHA-1318119A839687BF517823B2EA6850F13A529131F
SHA-2569FA6ED19F212ABCDED1BC313EA7F9B390450040FA0C98D76317BC047C2306799
Key Value
MD5E50F0163345661D73896C5E6908BF9C2
PackageArchs390
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease13.fc21
PackageVersion0.9.31
SHA-13925FC22754BEC7CECFB54ECF546923B068421A2
SHA-2560A8A9F4C6E8F27B3FE02F8C3CE74328FD2C1C9EF5BE9D3F729A48CC39E928B4B
Key Value
MD504B136D1C401BF252EC01A13A464ABDA
PackageArchppc64
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease11.fc20
PackageVersion0.9.31
SHA-13C263388AA59865AFEAA074A414B2B91F74B3B80
SHA-256C3FD4B2151B7A71BBA25725A225EE08FB72D19438ACFD3AC4803B1F0C4C38AD2
Key Value
MD577E0EF9448722FBADF5868B0E124F4E5
PackageArchppc64
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease14.fc22
PackageVersion0.9.31
SHA-14A9A0C4128E7602DDF385A82C5D746FD82C057FA
SHA-2569E19C8D30A6421489E50A1FC12C3228F36C5F6CBBDA4F73976BD70E2E7E58783
Key Value
MD55B1F2AD87990140BA08E1AFAD93D44ED
PackageArcharmv7hl
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease7.fc18
PackageVersion0.9.31
SHA-154C7921DFA6D6E544C90394244FFFD21E2883C9F
SHA-2568371F732F3AA4D044D41C1C3ACF0FD460A4CDAD0370E903F51CF5D8C5101A0EA
Key Value
MD58CBD4837FF171F0F531CA9F4D407E6DC
PackageArchppc
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerKoji
PackageNameR-Rsolid
PackageRelease6.fc17
PackageVersion0.9.31
SHA-156CC0597A5CF3E36CD10A7414693F78F9B24FC3A
SHA-2568F9864304C4DD03380BC226D816DB520B5B2CCCDBD74279513B33C0B8076CB87
Key Value
MD540C2FA8B9EE5AC322A23A1438EC09E00
PackageArchppc64
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerKoji
PackageNameR-Rsolid
PackageRelease7.fc18
PackageVersion0.9.31
SHA-15DDA0DADDABD1990C632AC12E4295C4DA0696A6B
SHA-2560B7304797AFFD4F0363548279450B06036FC42BCAF3E60C81B8BF9A7A4ADFEC7
Key Value
MD52DEB3D129989A527ECD6F537A56B7757
PackageArchs390
PackageDescription Rsolid is an R package for normalizing fluorescent intensity data from ABI/SOLiD second generation sequencing platform. It has been observed that the color-calls provided by factory software contain technical artifacts, where the proportions of colors called are extremely variable across sequencing cycles. Under the random DNA fragmentation assumption, these proportions should be equal across sequencing cycles and proportional to the dinucleotide frequencies of the sample. Rsolid implements a version of the quantile normalization algorithm that transforms the intensity values before calling colors. Results show that after normalization, the total number of mappable reads increases by around 5%, and number of perfectly mapped reads increases by 10%. Moreover a 2-5% reduction in overall error rates is observed, with a 2-6% reduction in the rate of valid adjacent color mis-matches. The latter is important, since it leads to a decrease in false-positive SNP calls. The normalization algorithm is computationally efficient. In a test we are able to process 300 million reads in 2 hours using 10 computer cluster nodes. The engine functions of the package are written in C for better performance.
PackageMaintainerFedora Project
PackageNameR-Rsolid
PackageRelease14.fc22
PackageVersion0.9.31
SHA-16FCA5AAD9A0ED81C9A6D6CD90F07F5F37C9E5F9D
SHA-256915E3769869AF82195B3C7410535F150560B55EB5C9B21DFD82398905F9CAFD6