Hi all
I am new entrant on this platform. I am a tyro on NGS analysis. What motivated me to come into this field is basically emergence of NGS data exponentially. Also presently my project is analyzing the RNA-seq data.
I want to align RNA-seq data (READS) of a experiment related to prostate cancer in human on the reference genome. I don't know which reference genome should I take for mapping upon. Is it right to take hg19 whole human genome from UCSC genome browser site ? OR should I take genome specific for prostate cancer only ?
Thanks in advance.
Kumardeep
I am new entrant on this platform. I am a tyro on NGS analysis. What motivated me to come into this field is basically emergence of NGS data exponentially. Also presently my project is analyzing the RNA-seq data.
I want to align RNA-seq data (READS) of a experiment related to prostate cancer in human on the reference genome. I don't know which reference genome should I take for mapping upon. Is it right to take hg19 whole human genome from UCSC genome browser site ? OR should I take genome specific for prostate cancer only ?
Thanks in advance.
Kumardeep
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