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7
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5
replies
2.9k
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Hypergeometric test's summary error while using GOstats
GO GOstats microarray enrichment
updated 4.6 years ago by 20 • written 6.5 years ago by ▴ 140
0
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0
replies
1.9k
views
Comment: C: Samtools fastq returns less unmapped than flagstat
5.2 years ago by ciemanek ▴ 140
2
votes
9
replies
1.9k
views
Samtools fastq returns less unmapped than flagstat
samtools ngs filtering alignment
updated 5.2 years ago by 20 • written 5.3 years ago by ▴ 140
0
votes
1
reply
1.9k
views
Comment: C: Samtools fastq returns less unmapped than flagstat
5.2 years ago by ciemanek ▴ 140
0
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0
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1.9k
views
Comment: C: Samtools fastq returns less unmapped than flagstat
5.3 years ago by ciemanek ▴ 140
0
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0
replies
1.9k
views
Comment: C: Samtools fastq returns less unmapped than flagstat
5.3 years ago by ciemanek ▴ 140
0
votes
1
reply
1.9k
views
Comment: C: Samtools fastq returns less unmapped than flagstat
5.3 years ago by ciemanek ▴ 140
0
votes
0
replies
2.5k
views
Comment: C: Filtering human reads in metagenomics: should supplementary reads be removed?
5.4 years ago by ciemanek ▴ 140
0
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1
reply
2.5k
views
Comment: C: Filtering human reads in metagenomics: should supplementary reads be removed?
5.4 years ago by ciemanek ▴ 140
1
vote
5
replies
2.5k
views
Filtering human reads in metagenomics: should supplementary reads be removed?
dna-seq metagenomics bwa samtools flagstat
5.4 years ago by ciemanek ▴ 140
10
votes
6
replies
2.4k
views
Forum: How to acknowledge in the paper a reference genome that hasn't been published yet?
reference paper
updated 18 months ago by 44k • written 6.3 years ago by ▴ 140
0
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1
reply
2.4k
views
Comment: C: How to acknowledge in the paper a reference genome that hasn't been published ye
6.3 years ago by ciemanek ▴ 140
1
vote
0
replies
2.9k
views
Answer: A: Hypergeometric test's summary error while using GOstats
6.4 years ago by ciemanek ▴ 140
0
votes
0
replies
1.9k
views
Comment: C: Categorize patients based on continuous variables
6.7 years ago by ciemanek ▴ 140
6
votes
7
replies
1.9k
views
Categorize patients based on continuous variables
biostatictics expression
updated 6.7 years ago by 15k • written 6.7 years ago by ▴ 140
1
vote
1
reply
1.9k
views
Comment: A: Categorize patients based on continuous variables
6.7 years ago by ciemanek ▴ 140
0
votes
1
reply
1.9k
views
Comment: C: Categorize patients based on continuous variables
6.7 years ago by ciemanek ▴ 140
1
vote
0
replies
2.3k
views
Comment: C: affy MAplot NA error
6.8 years ago by ciemanek ▴ 140
1
vote
2
replies
2.3k
views
affy MAplot NA error
affymetrix maplot microarrays affy quantile
updated 6.8 years ago by 88k • written 6.8 years ago by ▴ 140
2
votes
1
reply
1.4k
views
Mutations and copy number variations from DNA-Seq
SNP sequencing DNA-Seq CNV CNA
updated 6.9 years ago by ★ 2.3k • written 6.9 years ago by ▴ 140
4
votes
2
replies
1.3k
views
Mutation impact on DNA binding
protein modelling mutation proteomics
updated 6.9 years ago by 20 • written 7.0 years ago by ▴ 140
0
votes
0
replies
1.9k
views
Comment: C: Augustus gene on forward and reverse strain
7.2 years ago by ciemanek ▴ 140
0
votes
1
reply
1.9k
views
Comment: C: Augustus gene on forward and reverse strain
7.2 years ago by ciemanek ▴ 140
1
vote
4
replies
1.9k
views
Augustus gene on forward and reverse strain
gene prediction annotation augustus ngs
7.2 years ago by ciemanek ▴ 140
0
votes
0
replies
2.2k
views
How to integrate augustus and InterProScan annotation?
ngs annotation interproscan augustus
7.3 years ago by ciemanek ▴ 140
0
votes
0
replies
1.6k
views
How to get more information about variants in intergenic regions?
ngs annotation variants snpeff
7.3 years ago by ciemanek ▴ 140
0
votes
0
replies
1.8k
views
Combine VCF files with multiple alternative alleles in GATK
gatk combine ngs sequencing variants calling
7.4 years ago by ciemanek ▴ 140
2
votes
1
reply
3.3k
views
GATK VariantFiltration invalid expression
ngs gatk variants filtration
updated 7.4 years ago by 16k • written 7.4 years ago by ▴ 140
0
votes
0
replies
1.7k
views
Comment: C: snpEff: gene-CHR_END annotation
7.4 years ago by ciemanek ▴ 140
1
vote
2
replies
1.7k
views
snpEff: gene-CHR_END annotation
snp sequencing annotation snpeff
updated 7.4 years ago by 164k • written 7.4 years ago by ▴ 140
4
votes
1
reply
4.5k
views
Intersect multiple VCF files
SNP vcf intersect vcftools bedtools
updated 7.5 years ago by 20k • written 7.5 years ago by ▴ 140
0
votes
0
replies
4.9k
views
Comment: C: VCFtools intersect vs. GATK intersect
7.5 years ago by ciemanek ▴ 140
2
votes
2
replies
4.9k
views
VCFtools intersect vs. GATK intersect
snp sequencing gatk vctfools intersect
updated 7.5 years ago by 164k • written 7.5 years ago by ▴ 140
0
votes
0
replies
1.8k
views
Obtaining beads number from MethylSet (minfi)
minfi methylation 450k illumina R
8.2 years ago by ciemanek ▴ 140
0
votes
0
replies
3.4k
views
Comment: C: Methylation 450k data preprocessing using Python
8.3 years ago by ciemanek ▴ 140
2
votes
3
replies
3.4k
views
Methylation 450k data preprocessing using Python
methylation python rpy2 R preprocessing
updated 8.3 years ago by ▴ 810 • written 8.3 years ago by ▴ 140
0
votes
0
replies
3.8k
views
Comment: C: bwa aln for paired-end sequencing data in one .fastq file
8.3 years ago by ciemanek ▴ 140
0
votes
0
replies
3.8k
views
Comment: C: bwa aln for paired-end sequencing data in one .fastq file
8.3 years ago by ciemanek ▴ 140
0
votes
0
replies
3.8k
views
Comment: C: bwa aln for paired-end sequencing data in one .fastq file
8.3 years ago by ciemanek ▴ 140
6
votes
3
replies
6.7k
views
VarScan and Samtools - how to process my data?
ngs sequencing varscan samtools pipeline
updated 8.3 years ago by ★ 3.2k • written 8.3 years ago by ▴ 140
5
votes
7
replies
3.8k
views
bwa aln for paired-end sequencing data in one .fastq file
RNA-Seq alignment sequencing bwa aln
8.5 years ago by ciemanek ▴ 140
41 results • Page 1 of 1
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