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Discarding duplicate reads from fastq file on the basis of random barcode
sequencing next-gen gene
updated 4.4 years ago by 20 • written 4.6 years ago by ▴ 10
1
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0
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4.0k
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Comment: C: bowtie2 piped to samtools created many samtools.tmp.bam files, how to get the si
4.5 years ago by naeem40thju ▴ 10
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2.3k
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Comment: C: How can I count the number of UMIs and reads at each position after mapping with
4.5 years ago by naeem40thju ▴ 10
1
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7
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2.3k
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How can I count the number of UMIs and reads at each position after mapping with a reference sequence?
next-gen sequencing
4.5 years ago by naeem40thju ▴ 10
0
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1
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5.8k
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Comment: C: tool to analysis bulk RNAseq data with UMIs
updated 4.5 years ago by 148k • written 4.5 years ago by ▴ 10
0
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4
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1.3k
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How to cut some part of the header of reads in FASTQ file?
next-gen sequencing
updated 21 months ago by • 0 • written 4.5 years ago by ▴ 10
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0
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5.8k
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Comment: C: tool to analysis bulk RNAseq data with UMIs
4.5 years ago by naeem40thju ▴ 10
0
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0
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1.5k
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Comment: C: How can I count the barcodes of alligned reads at each position?
4.5 years ago by naeem40thju ▴ 10
0
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1
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1.5k
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Comment: C: How can I count the barcodes of alligned reads at each position?
4.5 years ago by naeem40thju ▴ 10
0
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1
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1.5k
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Comment: C: How can I count the barcodes of alligned reads at each position?
4.5 years ago by naeem40thju ▴ 10
0
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5
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1.5k
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How can I count the barcodes of alligned reads at each position?
next-gen sequencing
updated 4.5 years ago by 164k • written 4.5 years ago by ▴ 10
0
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1
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1.5k
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Comment: C: How can I extract the sequencing reads containing a specific linker/tag?
4.6 years ago by naeem40thju ▴ 10
3
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5
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1.5k
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How can I extract the sequencing reads containing a specific linker/tag?
sequencing next-gen
updated 4.6 years ago by 148k • written 4.6 years ago by ▴ 10
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