i have project to align 2 genome . Generated the reference index: bwa index reference.fa Then i want to align the reads to the reference index bwa mem reference.fa reads1.fq reads2.fq > aligned_pairs.sam To download the reads for the second genome , i use the genome deposit SRA accession number to download from ENA . the page present option : FASTQ files (FTP) NCBI SRA file (FTP file1 file1 file2 SRA accession number SRR1779159 which one should be used ?
Question: how i can use SRA accession Number to call raw reads ?
12 months ago by
sh_shaddad77 • 0
sh_shaddad77 • 0 wrote:
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