Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

gtf file for hg38_v0_chrM_Homo_sapiens_assembly38.chrM.fasta

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    Gökalp Çelik

    Hi again. 

    Mitochondria genome for the task should be compatible with the hg38 gencode annotations therefore gtf file should be ok. 

    Regards.

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