Result for 119152F4D3B8B48477EFFF10A0BAFFF6FD0C6D2D

Query result

Key Value
FileName./usr/lib64/R/library/Rsolid/Meta/data.rds
FileSize73
MD5306E8E897173655911052446FF3F2C5F
SHA-1119152F4D3B8B48477EFFF10A0BAFFF6FD0C6D2D
SHA-25685DD8FBF00B74DEED078CFAA73ADF0DB9242B1E2941D3C83DFC76929B877AC23
SSDEEP3:FttVFHsHjdm7apn51znXjxKI/7/n:XtVFG5m7aprzXjMI/7/n
TLSHT12FA022CCA3080282F022803280C02F03E00C0C82A38C2C8B088B03030200A03C20030C
hashlookup:parent-total6
hashlookup:trust80

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Parents (Total: 6)

The searched file hash is included in 6 parent files which include package known and seen by metalookup. A sample is included below:

Key Value
MD5CB198B2C878F488C0E4E1B1EEE6BC919
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
PackageRelease7.fc18
PackageVersion0.9.31
SHA-18BB5DEBBAF23AE5BEF12AFD0E4014DB9795F7026
SHA-256EF81DA7BC2F0D63FDD95690BA29660AD9568253A9D50FE06CEC5E099256C9A3F
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
MD50473B38CFA5B2D5A1F1B46D4222EEDC5
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
PackageRelease7.fc18
PackageVersion0.9.31
SHA-1996949DCD3C51AFDB520CBD7A3166E5AB9AD8BE1
SHA-2561094F1B71F884C69E2A414EF42CB3C50E8C7D97F6D57D81648F2A9029DEB80B8
Key Value
MD5F6649DCFD6D6683BDDB5A66D25769AC1
PackageArcharmv5tel
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-1D25F1780E765D20EB5C4915AD1AB2A915BADFDDD
SHA-2565D5A8BFB1EA368B67DC23B6BDE06A54331EFEC1CED6908600AB4C0A0C328EFDD
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
MD55FAA035B168601BE667E7634791C5925
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
PackageRelease7.fc18
PackageVersion0.9.31
SHA-1AA17349E9DC7650E4F023220DEA93919C05E47D3
SHA-256A31FC52E83D756055F1D2BCBA18F22971BDB6D505841804153A2AF76FE9BF5C5