Coverage analysis in a targeted amplicon-based next-generation sequencing panel

Hi folks,

Can anyone help me with an issue please?

I performed NGS sequencing of a custom panel (that I designed) from illumina (Truseq). Could you tell me which tools can I use to calculate the coverage in my desired regions? I tried GATK and bcftools but I can not do what I wanted.

Imagine I have 100 amplicons that I amplified for 95 samples, I would like to know how many reads there are per sample and per amplicon. Something like this:

                  sample1    sample2   sample3
amplicon1         100           45       20
amplicon2           0           10       5
amplicon2          80           57       90

I need to understand how the sequencing worked in my panel, if I have coverage in all amplicons or not.

Thanks in advance,

Ana

ngs illumina truseq coverage

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updated 9.8 years ago by Zaag

• written 9.8 years ago by armarkes •

Have you fix the problem? I have a suggestion. You can turn the bam file to bed file . The pair read's start and end will match the amplicon's start and end. So you can just count the reads whose start and end match the amplicon

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written 9.3 years ago by tiehan •

3 answers

Bedtools is a good option indeed. I can also recommend Picard Tool's CalculateHsMetrics tool which is very useful when analyzing the success of targeted NGS sequencing. It doesn't give the result you are exactly asking for but it reports the percentage of bases covered less than nX times in targeted sequencing. In other words it gives you an answer for question "How many percent of my bases is covered at least 100 times?" and so on. With an appropriate BED file it should be possible to evaluate the success of individual amplicons.

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written 9.8 years ago by Jokhe •

GATK's depth of coverage does exactly what you want. Give it all the BAM files and a bed file with the amplicon regions and it will give the coverage per region per patient, per base per patient and some more.

java -jar GenomeAnalysisTK.jar -T DepthOfCoverage -R ref.fa \
-I file1.bam \
-I file2.bam \
--countType COUNT_FRAGMENTS \
-o output \
-L target.bed

And the per target output will look like this (in table form):

| Target | total_coverage | average_coverage | file1_total_cvg | file1_mean_cvg | file1_granular_Q1 | file1_granular_median | file1_granular_Q3 | file1_%_above_15 | file2_total_cvg | file2_mean_cvg | file2_granular_Q1 | file2_granular_median | file2_granular_Q3 | file2_%_above_15 | |:--------------:|----------------|------------------|-----------------|----------------|-------------------|-----------------------|-------------------|------------------|-----------------|----------------|-------------------|-----------------------|-------------------|------------------| | chr1:1000-2000 | 1286996 | 10054.66 | 40746 | 318.33 | 328 | 328 | 328 | 100 | 43366 | 338.8 | 342 | 342 | 357 | 100 | | chr1:4000-4500 | 1907320 | 10422.51 | 56206 | 307.14 | 314 | 314 | 328 | 100 | 60442 | 330.28 | 314 | 342 | 357 | 100 |

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written 9.8 years ago by Zaag

Thanks a lot for your help. I already tried this option but I got the coverage per each base instead of the coverage per amplicon. I created a bed file with coordinates for each amplicon, but the tool calculates coverage per site, instead of coverage per region. Maybe I am missing some option, but I do not know what it is. Do you know how to handle it?

Thanks in advance. Ana

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written 9.8 years ago by armarkes •

I get a per base file and: