I have human Exome data aligned to the GrCh37 reference as BAM files. Enriched regions are also available as a bed file. I need to get, up to what percentage the "supposed to be enriched regions" are actually covered and in what depth.
For ex:
Coverage at 10x = 95% Coverage at 20x = 90% Coverage at 30x = 86%
qualimap can generate a report as you wanted.
Simple command: qualimap bamqc -bam you_bam_file.bam -outfile report.pdf -outformat PDF
A portion of the report for example:
>>>>>>> Coverage
mean coverageData = 32.3065X
std coverageData = 48.0755X
There is a 75.49% of reference with a coverageData >= 1X
There is a 71.4% of reference with a coverageData >= 2X
There is a 68.41% of reference with a coverageData >= 3X
There is a 65.65% of reference with a coverageData >= 4X
There is a 63.03% of reference with a coverageData >= 5X
There is a 60.5% of reference with a coverageData >= 6X
There is a 58.11% of reference with a coverageData >= 7X
There is a 55.96% of reference with a coverageData >= 8X
There is a 54.04% of reference with a coverageData >= 9X
There is a 52.34% of reference with a coverageData >= 10X
There is a 50.84% of reference with a coverageData >= 11X
There is a 49.49% of reference with a coverageData >= 12X
There is a 48.32% of reference with a coverageData >= 13X
There is a 47.23% of reference with a coverageData >= 14X
There is a 46.25% of reference with a coverageData >= 15X
There is a 45.37% of reference with a coverageData >= 16X
There is a 44.57% of reference with a coverageData >= 17X
There is a 43.83% of reference with a coverageData >= 18X
There is a 43.12% of reference with a coverageData >= 19X
There is a 42.43% of reference with a coverageData >= 20X
There is a 41.8% of reference with a coverageData >= 21X
There is a 41.18% of reference with a coverageData >= 22X
There is a 40.57% of reference with a coverageData >= 23X
There is a 39.99% of reference with a coverageData >= 24X
There is a 39.42% of reference with a coverageData >= 25X
There is a 38.87% of reference with a coverageData >= 26X
There is a 38.34% of reference with a coverageData >= 27X
There is a 37.81% of reference with a coverageData >= 28X
There is a 37.29% of reference with a coverageData >= 29X
There is a 36.78% of reference with a coverageData >= 30X
There is a 36.28% of reference with a coverageData >= 31X
There is a 35.79% of reference with a coverageData >= 32X
There is a 35.3% of reference with a coverageData >= 33X
There is a 34.81% of reference with a coverageData >= 34X
There is a 34.32% of reference with a coverageData >= 35X
There is a 33.84% of reference with a coverageData >= 36X
There is a 33.36% of reference with a coverageData >= 37X
There is a 32.89% of reference with a coverageData >= 38X
There is a 32.41% of reference with a coverageData >= 39X
There is a 31.93% of reference with a coverageData >= 40X
There is a 31.46% of reference with a coverageData >= 41X
There is a 30.98% of reference with a coverageData >= 42X
There is a 30.52% of reference with a coverageData >= 43X
There is a 30.04% of reference with a coverageData >= 44X
There is a 29.57% of reference with a coverageData >= 45X
There is a 29.1% of reference with a coverageData >= 46X
There is a 28.62% of reference with a coverageData >= 47X
There is a 28.14% of reference with a coverageData >= 48X
There is a 27.65% of reference with a coverageData >= 49X
There is a 27.17% of reference with a coverageData >= 50X
There is a 26.68% of reference with a coverageData >= 51X
What kind of data do you have, and what are you trying to accomplish?
I have human Exome data aligned to the GrCh37 reference as BAM files. Enriched regions are also available as a bed file. I need to get, up to what percentage the "supposed to be enriched regions" are actually covered and in what depth.
For ex:
Coverage at 10x = 95% Coverage at 20x = 90% Coverage at 30x = 86%
See: depth calculation for targeted resequencing