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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Junior Member
Location: Germany Join Date: Mar 2020
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I have a bed file of some custom regions I have interest in, e.g.
chr1 1000 1015 my_region 0 + ... I believe these regions may be translated, but are not necessarily annotated genes. So I would like to map some reads to these regions to confirm my suspicions. The dataset GSE109313 has 1 Trillion reads from various human tissues. Clicking on the run selector I can see the 37 SRR samples. Using Code:
prefetch Often reads are mapped to a GTF file, e.g. the human GTF file can be found on ensembl. So now I have bed file or regions I would like to map to, the human GTF file, and the ~400Gb of SRR files. Where do I go from here? |
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Tags |
gtf annotation file, how-to, howto, mapping reads, next-gen sequencing |
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