ctDNAtools

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Hi, Thanks for a great tool! I am trying to use test_ctDNA on bam files from targeted panel sequencing data and with BAM files aligned to RefSeq: NCBI GRCH37 Reference...

zahrahaider

How to know the shared mutations in test_ctDNA()

3

Hi, Thank you for this tools ... I have a question please , Is there a way to know the mutations shared in between the tumour and ctDNA in positive...

esraa-jamal

Detailed results

1

Hello and thank you for your work, I find it very interesting! I would like to know if it's possible to provide more details about the output of the test_ctdna()...

aleest21

bfs counts always 0

2

Hi! All the counts from the bfs are NaN when normalized and 0 when not normalized. Below is the code I ran: ``` `> bfs % + map(bin_fragment_size, bin_size =...

rpauly

Dear Amjad Alkodsi, I am a bioinformatician, and I was wondering if is it possible to use un-matched healthy samples respect to the tumor samples that we sequenced. We cannot...

frasca17