Hi all , I am working on RNA -seq Data analysis. I have reads for specific gene in a bam format which I was extracted using samtools command. That bam file contain 37 reads. I want merge these overlap reads and make into single file. Is there any tool available to do this ? Pls let me know ? (It is a pair end seq reads).
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Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
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Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
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