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10
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2
answers
173
views
6 follow
2
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Which repository is more appropriate to submit for cancer cell line (bulk) RNA-seq data ?
rna-seq written 10 weeks ago by arta520 • updated 3 hours ago by Biostar ♦♦ 20
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34
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0
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8
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0
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182
views
0
answers
0
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0
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39
views
0
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Using RepeatModeler for novel assembled genome
genome assembly repeatmodeler written 13 hours ago by nehleen110 • updated 6 hours ago by WouterDeCoster31k
1
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1
answer
39
views
1
answer
2
votes
1
answer
74
views
1
answer
4
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1
answer
2.3k
views
1
answer
Merging And De-Duplicating Structural Variant Calls (Bedpe)
intersect structural written 7.1 years ago by Stephane Plaisance370 • updated 9 hours ago by Biostar ♦♦ 20
1
vote
1
answer
58
views
1
answer
Giga base or Giga byte
gb assembly coverage written 10 hours ago by Shawrob4000
0
votes
1
answer
75
views
1
answer
9
votes
1
answer
91
views
1
answer
Forum: How to acknowledge in the paper a reference genome that hasn't been published yet?
paper forum reference written 18 hours ago by ciemanek100 • updated 11 hours ago by genomax54k
2
votes
0
answers
338
views
0
answers
0
votes
1
answer
38
views
1
answer
autosomal ancestry inference
gwas ancestry written 14 hours ago by J.F.Jiang710 • updated 12 hours ago by Kevin Blighe25k
0
votes
3
answers
947
views
3
answers
RepeatModeler cannot be run in parallel
repeatmodeler repeatmasker written 23 months ago by tlorin240 • updated 13 hours ago by nehleen110
0
votes
1
answer
103
views
1
answer
How group merged VCFs in one GT column
vcf bcftools written 1 day ago by miqrom0 • updated 13 hours ago by Kevin Blighe25k
0
votes
0
answers
32
views
0
answers
371
votes
17
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26k
views
170 follow
17
answers
News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 20 months ago by Istvan Albert ♦♦ 77k • updated 13 hours ago by Fanta0
4
votes
1
answer
117
views
5 follow
1
answer
Very low unique mapped reads - STAR alignment
rna-seq written 1 day ago by junsionglow20 • updated 14 hours ago by h.mon18k
0
votes
0
answers
37
views
0
answers
remove primer sequences from BAM file
bam primer written 14 hours ago by J.F.Jiang710
2
votes
0
answers
91
views
0
answers
Forum: TACC vs SDSC vs HTCondor
forum pbs written 21 days ago by Shicheng Guo6.1k • updated 15 hours ago by h.mon18k
4
votes
0
answers
136
views
5 follow
0
answers
Issue with Samtools variant calling
genome assembly alignment written 7 weeks ago by williamsbrian506490 • updated 15 hours ago by Biostar ♦♦ 20
4
votes
2
answers
106
views
2
answers
Identifying covered genes from nanopore cDNA-seq reads
gene alignment rna-seq written 1 day ago by florian.bernard510 • updated 16 hours ago by WouterDeCoster31k
0
votes
0
answers
821
views
0
answers
How to detect segmental duplications?
genome assembly alignment written 23 months ago by lamz13813840 • updated 17 hours ago by WouterDeCoster31k
4
votes
4
answers
138
views
5 follow
4
answers
How to get PCA3 and PCA4 from Deseq2?
rna-seq written 1 day ago by morteza.khabiri0 • updated 22 hours ago by cpad01128.3k
0
votes
0
answers
30
views
0
answers
0
votes
1
answer
48
views
1
answer
VCF to Bed file format using GATK
vcf gatk rna-seq bed written 1 day ago by Sa0 • updated 23 hours ago by chrchang5233.7k
8
votes
3
answers
2.2k
views
7 follow
3
answers
how can i remove duplicated variants from vcf file?
vcf snp written 12 months ago by kk.mahsa70 • updated 23 hours ago by Shicheng Guo6.1k
1
vote
2
answers
82
views
2
answers
0
votes
1
answer
63
views
1
answer
Database of Mutations and the associated drugs
ngs wes written 1 day ago by Ron800 • updated 1 day ago by Kevin Blighe25k
3
votes
1
answer
579
views
1
answer
Confused about data sets for SVM algorithm
svm molecules support vector machine written 2.0 years ago by spacegeek121230 • updated 1 day ago by Biostar ♦♦ 20
3
votes
0
answers
57
views
0
answers
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