Download the ebook and commands here: www.patreon.com/posts/genome-mapping-78145935
@velamuriishwarya7100
7 ай бұрын
Thank you. It was really helpful.
@user-tm9di3ot3x
Жыл бұрын
Thanks for the bioinfromatics videos. Have you got video about structural variation calling?
@junaidyousaf9240
10 ай бұрын
After this video, which video should I watch for stats in R
@serychristianrenaud
Жыл бұрын
Thank
@ceci5393
Жыл бұрын
Really useful to me all your videos!! thanks a lot!! very clear. I would like to filter the reads mapped. Which is the tutorial where you explain this? Thank you again and greetings from Argentina 😊
@bioinformaticscoach
Жыл бұрын
At the moment, there is one video.kzitem.info/news/bejne/ooSh2JptpJp5YKw I am working on other filtering videos. But if you need help urgently , you can book a session with me clarity.fm/search/vincentappiah
@ceci5393
Жыл бұрын
@@bioinformaticscoach Thank you very much for your answer! I´m going to do it now!
@bioinformaticscoach
Жыл бұрын
@@ceci5393 here is the link to book a session: clarity.fm/search/vincentappiah
@abelinoskosmos1679
Жыл бұрын
is there a way to make the output in fastq.gz format instead of .SAM? thanks
@bioinformaticscoach
Жыл бұрын
Yes. It's possible. You can use samtools to do that.
@wemakecreators3101
Жыл бұрын
I have my owm fungus sequencing data I tried doing same with my data and alingmemt rate comes out 1.12%
@bioinformaticscoach
Жыл бұрын
You need to make sure you are using the correct reference sequence. You can also do QC to check if you have enough reads
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