Understanding VCF file | Variant Call Format Part 1/3

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LiquidBrain Bioinformatics

LiquidBrain Bioinformatics

Күн бұрын

Пікірлер: 18
@maraoz
@maraoz 3 жыл бұрын
I've been lost trying to understand differences between FASTA, FASTQ, VCF, and CRAM for some days now, and I finally get it. thanks for this video!
@emetitiri
@emetitiri 3 жыл бұрын
Really appreciate this series, thanks! Your descriptions are clear and easy to understand.
@tethpheak6745
@tethpheak6745 2 ай бұрын
Thank you so much for your kind sharing
@HaileG-2020
@HaileG-2020 10 ай бұрын
How to convert numerical GT format to letter or nucleotide GT format???
@jinayenamin6676
@jinayenamin6676 3 жыл бұрын
This was very helpful. Thanks :)
@elenips7231
@elenips7231 2 жыл бұрын
Very helpful video , thank you!! I am not really familiar with bioinformatics and in this part of my project, I am trying two compare two VCF files corresponding to the results of healthy tissue and tumor tissue. I want to compare these VCF files and remove their similarities. More specific I want to remove the information of the healthy tissue from the tumor one. Have you any suggestions on which tool I should use or any way that I can do my analysis? thank you in advance!
@chesterhung6154
@chesterhung6154 3 жыл бұрын
How about translocation? Translocation is another form of structural variation where non homologous chromosomes break apart and rejoin back to each other chromosomes by DNA repair machinery.
@sketchgamma
@sketchgamma 3 жыл бұрын
Thanks dude
@kadidyasmine8775
@kadidyasmine8775 3 жыл бұрын
Hello Am currenly working on a theme: use of neural network to identify somatic variations, i would ask you if u have an idea from where can i get suitable dataset Thank you
@LiquidBrain
@LiquidBrain 3 жыл бұрын
Are you looking for fastq? I usually look at SRA for those raw data
@taniadas3301
@taniadas3301 2 жыл бұрын
Any tutorial on how to parse a vcf file in python\ R?
@Dezzy7model
@Dezzy7model Жыл бұрын
probably late but for R use vcfR package.
@chaofang9576
@chaofang9576 4 жыл бұрын
great,are you malaysia?
@LiquidBrain
@LiquidBrain 4 жыл бұрын
Yap, I am Malaysian
@chaofang9576
@chaofang9576 4 жыл бұрын
@@LiquidBrain thank you for your video ,later maybe you will introduction gatk?
@marwanmahmoodsaleh8088
@marwanmahmoodsaleh8088 3 жыл бұрын
Hello I had done the whole genome sequence by NGS (Illumina) of the bacteria. The files I received from the company are Fastaq1, Fastaq2, Filtered 1 Fastq Filtered 2 Fastq and analysis results file include :rmdup.bam.bai, rmdup.bam, filtered vcf and annotated vcf. Please tell me which of these files should be converted to FASTA and submitted to NCBI? Thanks
@LiquidBrain
@LiquidBrain 3 жыл бұрын
that really depends where you submitting to, is it SRA?
@marwanmahmoodsaleh8088
@marwanmahmoodsaleh8088 3 жыл бұрын
@@LiquidBrain I want to registr this sequence. May be SRA or others that can you guide me.
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