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7
votes
7
replies
9.2k
views
Filtering lowly expressed genes - edgeR
filtering RNA-Seq R edgeR
updated 4.1 years ago by ▴ 40 • written 6.9 years ago by ▴ 130
0
votes
0
replies
1.1k
views
proteins.actions file of string
string network
6.6 years ago by noeD ▴ 130
0
votes
1
reply
1.9k
views
smallRNA alignment and counting multimapping
smallRNA alignment featurescount
updated 7.0 years ago by 9.0k • written 7.0 years ago by ▴ 130
3
votes
1
reply
5.3k
views
dbsnp hg 38
dbsnp hg38 gatk baseRecalibrator
updated 7.1 years ago by 16k • written 7.1 years ago by ▴ 130
1
vote
1
reply
1.4k
views
variant Recalibrator, -an option
GATK VARIANT RECALIBRATOR -an
updated 7.1 years ago by 164k • written 7.1 years ago by ▴ 130
0
votes
0
replies
1.4k
views
locateVariants missing some mutation site
R Bioconductor Variant Annotation
7.1 years ago by noeD ▴ 130
0
votes
1
reply
2.9k
views
Comment: C: Cosmic Database using BioMart
7.1 years ago by noeD ▴ 130
5
votes
3
replies
2.9k
views
Cosmic Database using BioMart
R BioMart Cosmic
updated 7.1 years ago by 24k • written 7.1 years ago by ▴ 130
0
votes
1
reply
2.7k
views
Comment: C: featuresCount -s 2 option
7.3 years ago by noeD ▴ 130
0
votes
1
reply
2.7k
views
Comment: C: featuresCount -s 2 option
7.3 years ago by noeD ▴ 130
6
votes
7
replies
2.7k
views
featuresCount -s 2 option
featuresCount RNA-Seq
updated 7.3 years ago by 104k • written 7.3 years ago by ▴ 130
0
votes
0
replies
5.2k
views
Comment: C: extract subset of sequence
7.3 years ago by noeD ▴ 130
0
votes
1
reply
31k
views
Comment: C: Bowtie2 parameters for best alignment
7.3 years ago by noeD ▴ 130
0
votes
0
replies
5.1k
views
Comment: C: featuresCount order sam file?
7.3 years ago by noeD ▴ 130
1
vote
1
reply
5.1k
views
Comment: C: featuresCount order sam file?
7.3 years ago by noeD ▴ 130
0
votes
1
reply
5.1k
views
Comment: C: featuresCount order sam file?
7.3 years ago by noeD ▴ 130
0
votes
1
reply
5.1k
views
Comment: C: featuresCount order sam file?
7.3 years ago by noeD ▴ 130
7
votes
9
replies
5.1k
views
featuresCount order sam file?
featuresCount RNA-Seq gtf sort
updated 7.3 years ago by 35k • written 7.3 years ago by ▴ 130
4
votes
2
replies
2.1k
views
smallRNA low percentage of mapping, N at the beninning of the reads and kmers
smallRNA RNA-Seq alignment
updated 7.3 years ago by 20k • written 7.3 years ago by ▴ 130
1
vote
0
replies
4.3k
views
Comment: C: non coding smallRNA annotation gtf file
7.4 years ago by noeD ▴ 130
0
votes
1
reply
4.3k
views
Comment: C: non coding smallRNA annotation gtf file
7.4 years ago by noeD ▴ 130
0
votes
1
reply
4.3k
views
Comment: C: non coding smallRNA annotation gtf file
7.4 years ago by noeD ▴ 130
1
vote
6
replies
4.3k
views
non coding smallRNA annotation gtf file
smallRNA gtf annotation
7.4 years ago by noeD ▴ 130
0
votes
0
replies
14k
views
Comment: C: Finding total number of reads from BAM file
7.6 years ago by noeD ▴ 130
0
votes
1
reply
14k
views
Comment: C: Finding total number of reads from BAM file
7.6 years ago by noeD ▴ 130
2
votes
0
replies
1.8k
views
Comment: C: Where can I find a sample analysis pipeline for DNA?
7.6 years ago by noeD ▴ 130
0
votes
1
reply
1.8k
views
Comment: C: Where can I find a sample analysis pipeline for DNA?
7.6 years ago by noeD ▴ 130
0
votes
0
replies
4.0k
views
Answer: A: extract sample DP values from VCF
7.7 years ago by noeD ▴ 130
0
votes
0
replies
6.9k
views
Comment: C: compute coverage with file.bam and bed : bedtools empty output
7.7 years ago by noeD ▴ 130
0
votes
0
replies
4.0k
views
Comment: C: extract sample DP values from VCF
7.7 years ago by noeD ▴ 130
0
votes
1
reply
6.9k
views
Comment: C: compute coverage with file.bam and bed : bedtools empty output
7.7 years ago by noeD ▴ 130
0
votes
0
replies
6.9k
views
Comment: C: compute coverage with file.bam and bed : bedtools empty output
7.7 years ago by noeD ▴ 130
3
votes
6
replies
6.9k
views
compute coverage with file.bam and bed : bedtools empty output
coverage bed bam bedtools
updated 7.7 years ago by 104k • written 7.7 years ago by ▴ 130
4
votes
0
replies
4.1k
views
Comment: C: How can I input a BAM file to the samtools mpileup command without using a text
7.7 years ago by noeD ▴ 130
0
votes
0
replies
1.9k
views
Comment: C: TopHat2: --read-realign-edit-dist = 0 or default options?
7.8 years ago by noeD ▴ 130
0
votes
1
reply
1.9k
views
Comment: C: TopHat2: --read-realign-edit-dist = 0 or default options?
7.8 years ago by noeD ▴ 130
0
votes
4
replies
1.9k
views
TopHat2: --read-realign-edit-dist = 0 or default options?
tophat2 RNA-Seq alignment
7.8 years ago by noeD ▴ 130
0
votes
0
replies
2.1k
views
Comment: C: variant calling tumor/normal exome sequencing
7.8 years ago by noeD ▴ 130
0
votes
1
reply
2.1k
views
Comment: C: variant calling tumor/normal exome sequencing
7.9 years ago by noeD ▴ 130
0
votes
4
replies
2.1k
views
variant calling tumor/normal exome sequencing
variant calling exom sequencing
updated 7.9 years ago by 7.3k • written 7.9 years ago by ▴ 130
40 results • Page 1 of 1
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