Difference between revisions of "BaseQualityCheck"
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'''Algorithm''': | '''Algorithm''': | ||
| − | It read SAM/BAM file line by line | + | It read SAM/BAM file line by line. Then according to CIGAR string, it compares the alignment to reference genome (base by base) and record match and mismatch frequencies grouped by observed base quality. |
| − | The output will be observed quality (generated by Illumina machine) and empirical quality ( | + | The output will be observed quality (generated by Illumina machine) and empirical quality (calculated by Prob(Mismatch bases | base quality Q) = (Total number of mismatched bases with base quality Q) / (Total number of bases with base quality Q)), both in Phred quality score. |
| − | + | ||
| + | By default, we omit soft clips, insertion and deletion. | ||
| + | |||
| + | Note, we strongly recommend excluding dbSNP sites, or else you are likely to underestimate empirical quality. The program can read a plain text file to specify dbSNP positions via '-s' option. | ||
'''Syntax''': | '''Syntax''': | ||
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-q -> alignment with less than minimum mapping quality will not be counted | -q -> alignment with less than minimum mapping quality will not be counted | ||
-r -> reference genome (in KARMA format) | -r -> reference genome (in KARMA format) | ||
| − | -s -> load SNP positions from the file. It may either be a text file with chr/index pairs, one per line, or you may use a file created from mkgenomevector (binary memory mapped file). For NCBI 37, a sample dbSNP file is located in /home/bingshan/data/db/dbSNP130.UCSC.coordinates.tbl | + | -s -> load SNP positions from the file. It may either be a text file with chr/index pairs, using 1-index position, one per line, or you may use a file created from mkgenomevector (binary memory mapped file). For NCBI 37, a sample dbSNP file is located in /home/bingshan/data/db/dbSNP130.UCSC.coordinates.tbl |
-v -> output SAM record in which mismatched bases exist | -v -> output SAM record in which mismatched bases exist | ||
Thank '''Bingshan''' for his qPlot program and his input to finish this program. | Thank '''Bingshan''' for his qPlot program and his input to finish this program. | ||
Revision as of 22:50, 11 May 2010
Base Quality Check
(May 11, 2010 - Paul, Xiaowei)
Location: $(repository)/baseQualityCheck/baseQualityCheck
Algorithm:
It read SAM/BAM file line by line. Then according to CIGAR string, it compares the alignment to reference genome (base by base) and record match and mismatch frequencies grouped by observed base quality. The output will be observed quality (generated by Illumina machine) and empirical quality (calculated by Prob(Mismatch bases | base quality Q) = (Total number of mismatched bases with base quality Q) / (Total number of bases with base quality Q)), both in Phred quality score.
By default, we omit soft clips, insertion and deletion.
Note, we strongly recommend excluding dbSNP sites, or else you are likely to underestimate empirical quality. The program can read a plain text file to specify dbSNP positions via '-s' option.
Syntax:
baseQualityCheck [-c max record count] [-q minimumMapQuality] [-r reference] [-s dbSNP file] [-v] -c -> only process first (max record count). -q -> alignment with less than minimum mapping quality will not be counted -r -> reference genome (in KARMA format) -s -> load SNP positions from the file. It may either be a text file with chr/index pairs, using 1-index position, one per line, or you may use a file created from mkgenomevector (binary memory mapped file). For NCBI 37, a sample dbSNP file is located in /home/bingshan/data/db/dbSNP130.UCSC.coordinates.tbl -v -> output SAM record in which mismatched bases exist
Thank Bingshan for his qPlot program and his input to finish this program.
