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0
votes
2
replies
201
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  Most stringent settings for bwa mem
alignment bwa dna
updated 11 weeks ago by 88k • written 11 weeks ago by ▴ 90
0
votes
0
replies
430
views
Comment:  Comment: What is the most accurate short (ish) read aligner?
12 weeks ago by nanana ▴ 90
1
vote
5
replies
430
views
  What is the most accurate short (ish) read aligner?
aligner sequencing bwa minimap2
updated 11 weeks ago by 88k • written 12 weeks ago by ▴ 90
0
votes
1
reply
1.2k
views
  Get total trinucleotide counts from a subset of chromosomes
R genome
updated 2.8 years ago by 20 • written 3.9 years ago by ▴ 90
4
votes
2
replies
1.8k
views
  Normalise read counts between two bam files
genome next-gen sequencing
3.3 years ago by nanana ▴ 90
0
votes
0
replies
1.8k
views
Comment:  C: Normalise read counts between two bam files
3.3 years ago by nanana ▴ 90
0
votes
0
replies
884
views
  CNV-Seq read count normalisation
genome next-gen
3.3 years ago by nanana ▴ 90
0
votes
1
reply
1.9k
views
  Calculate allele frequency for structural variant breakpoints
genome next-gen
3.4 years ago by nanana ▴ 90
1
vote
0
replies
1.4k
views
Answer:  A: Future direction of Gene Set Enrichment Analysis
3.9 years ago by nanana ▴ 90
0
votes
0
replies
1.6k
views
Comment:  C: How to compare a tumour sample to multiple normal samples in Freebayes
3.9 years ago by nanana ▴ 90
1
vote
2
replies
1.6k
views
  How to compare a tumour sample to multiple normal samples in Freebayes
next-gen snp genome
updated 3.9 years ago by ▴ 70 • written 4.0 years ago by ▴ 90
0
votes
0
replies
1.5k
views
Comment:  C: Exclude reads soft-clipped > N bases in Freebayes
3.9 years ago by nanana ▴ 90
7
votes
6
replies
1.9k
views
  Calculate the fraction of genome that is feature X
R genome
3.9 years ago by nanana ▴ 90
0
votes
1
reply
3.0k
views
  Tools to filter Mutect2 output
genome SNP
3.9 years ago by nanana ▴ 90
0
votes
0
replies
1.9k
views
Comment:  C: Calculate the fraction of genome that is feature X
3.9 years ago by nanana ▴ 90
0
votes
1
reply
1.9k
views
Comment:  C: Calculate the fraction of genome that is feature X
3.9 years ago by nanana ▴ 90
0
votes
0
replies
1.2k
views
Answer:  A: Get total trinucleotide counts from a subset of chromosomes
3.9 years ago by nanana ▴ 90
1
vote
1
reply
1.0k
views
  Group mutations in SNP data
SNP genome
4.0 years ago by nanana ▴ 90
1
vote
0
replies
1.5k
views
Comment:  C: Exclude reads soft-clipped > N bases in Freebayes
4.0 years ago by nanana ▴ 90
0
votes
2
replies
1.5k
views
Comment:  C: Exclude reads soft-clipped > N bases in Freebayes
4.0 years ago by nanana ▴ 90
3
votes
6
replies
1.5k
views
  Exclude reads soft-clipped > N bases in Freebayes
next-gen snp
updated 4.0 years ago by 88k • written 4.0 years ago by ▴ 90
0
votes
0
replies
3.8k
views
Comment:  C: annotation of SV (Structural Variants)
4.0 years ago by nanana ▴ 90
0
votes
2
replies
1.0k
views
Comment:  C: Enrichment of genomic feature in DNA breakpoints
4.0 years ago by nanana ▴ 90
0
votes
1
reply
1.0k
views
Comment:  C: Enrichment of genomic feature in DNA breakpoints
4.0 years ago by nanana ▴ 90
0
votes
5
replies
1.0k
views
  Enrichment of genomic feature in DNA breakpoints
genome next-gen
4.0 years ago by nanana ▴ 90
8
votes
4
replies
5.4k
views
  Go In Non-Model Organisms
rna-seq gene-ontology
updated 7.4 years ago by ▴ 520 • written 7.4 years ago by ▴ 90
1
vote
1
reply
5.4k
views
Comment:  C: Go In Non-Model Organisms
7.4 years ago by nanana ▴ 90
27 results • Page 1 of 1
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