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Comment:
Comment: Don't see uploaded files for linking in EGA (European Genome Archive)
20 months ago by
optimistsso4co3
▴ 140
0
votes
1
reply
2.8k
views
Comment:
Comment: Singularity image is not working in nextflow
21 months ago by
optimistsso4co3
▴ 140
0
votes
2
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2.8k
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Comment:
Comment: Singularity image is not working in nextflow
21 months ago by
optimistsso4co3
▴ 140
0
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1
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949
views
Comment:
Comment: How to interpret deletion the length of chromosome?
2.0 years ago by
optimistsso4co3
▴ 140
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0
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1.6k
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Comment:
Comment: How to filter VCF for only variants present in particular sample?
2.5 years ago by
optimistsso4co3
▴ 140
0
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1
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1.6k
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Comment:
Comment: How to filter VCF for only variants present in particular sample?
2.5 years ago by
optimistsso4co3
▴ 140
0
votes
0
replies
1.3k
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Comment:
Comment: Is it possible to query column of particular sample on VCF?
2.5 years ago by
optimistsso4co3
▴ 140
0
votes
1
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1.3k
views
Comment:
Comment: Is it possible to query column of particular sample on VCF?
2.5 years ago by
optimistsso4co3
▴ 140
0
votes
1
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1.3k
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Comment:
Comment: Is it possible to query column of particular sample on VCF?
2.5 years ago by
optimistsso4co3
▴ 140
0
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0
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1.1k
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Comment:
Comment: Research Scientist (Fungal & Algal Program)
2.6 years ago by
optimistsso4co3
▴ 140
0
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0
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768
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Comment:
Comment: Mobile element discovery with MELT brings different results when chromosomes are
2.6 years ago by
optimistsso4co3
▴ 140
0
votes
0
replies
1.1k
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Comment:
Comment: How to correct for allele frequency mismatches?
3.0 years ago by
optimistsso4co3
▴ 140
1
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2.0k
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Comment:
Comment: Why isn't it a common practice to call variant for every position in human genom
3.1 years ago by
optimistsso4co3
▴ 140
0
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0
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2.0k
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Comment:
Comment: Why isn't it a common practice to call variant for every position in human genom
3.1 years ago by
optimistsso4co3
▴ 140
0
votes
1
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2.0k
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Comment:
Comment: Why isn't it a common practice to call variant for every position in human genom
3.1 years ago by
optimistsso4co3
▴ 140
0
votes
1
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2.0k
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Comment:
Comment: Why isn't it a common practice to call variant for every position in human genom
3.1 years ago by
optimistsso4co3
▴ 140
0
votes
0
replies
860
views
Comment:
Comment: Wha does combineGVCFs does to loci with variant only in gVCF from another analys
3.2 years ago by
optimistsso4co3
▴ 140
0
votes
1
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1.4k
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Comment:
Comment: What are "must have" data types one should extract from WGS .fq data?
3.2 years ago by
optimistsso4co3
▴ 140
0
votes
1
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1.4k
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Comment:
Comment: What are "must have" data types one should extract from WGS .fq data?
3.2 years ago by
optimistsso4co3
▴ 140
0
votes
1
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976
views
Comment:
Comment: Is it ok to replace missing WGS calls with reference notation "0/0"?
3.2 years ago by
optimistsso4co3
▴ 140
0
votes
1
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2.3k
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Comment:
Comment: How to pass custom software specific variables to nf-core/sarek nextflow pipelin
3.5 years ago by
optimistsso4co3
▴ 140
0
votes
2
replies
2.3k
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Comment:
Comment: How to pass custom software specific variables to nf-core/sarek nextflow pipelin
3.5 years ago by
optimistsso4co3
▴ 140
0
votes
0
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1.4k
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Comment:
Comment: How to paralle trim_galore for single sample?
3.5 years ago by
optimistsso4co3
▴ 140
0
votes
0
replies
3.4k
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Comment:
C: GTEX - how to upload more than one rsIDs to get gene expression or eQTL informat
4.3 years ago by
optimistsso4co3
▴ 140
0
votes
0
replies
1.9k
views
Comment:
C: Whats the point of genotype pruning before imputation?
5.5 years ago by
optimistsso4co3
▴ 140
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