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Comment:
Comment: gtf2bed doesn't give gene_id in the bed file
2.5 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
2.7k
views
Comment:
C: How I can reduce the depth of a sequencing when I want to assemble it?
updated 5.2 years ago by
Ram
44k • written 9.2 years ago by
stolarek.ir
▴ 700
1
vote
0
replies
5.3k
views
Comment:
C: Heatmap of Differentially Expressed Genes
updated 5.2 years ago by
Ram
44k • written 9.2 years ago by
stolarek.ir
▴ 700
1
vote
0
replies
6.8k
views
Comment:
C: How to convert Affymetrix SNP IDs to dbSNP rs SNP names
updated 5.2 years ago by
Ram
44k • written 9.3 years ago by
stolarek.ir
▴ 700
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votes
0
replies
6.2k
views
Comment:
C: Merging files in plink
6.9 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
3.4k
views
Comment:
C: Illumina paired end read header difference- SPAdes bwa run ERROR
7.4 years ago by
stolarek.ir
▴ 700
0
votes
0
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3.5k
views
Comment:
C: RNASeq lane effect
7.4 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
5.2k
views
Comment:
C: long reads Pacbio SNP calling
7.4 years ago by
stolarek.ir
▴ 700
2
votes
0
replies
13k
views
Comment:
C: Paired vs unpaired (DNA Sequencing)
7.5 years ago by
stolarek.ir
▴ 700
0
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1
reply
2.5k
views
Comment:
C: How to align multiple genomic regions simultaneously
7.5 years ago by
stolarek.ir
▴ 700
1
vote
1
reply
2.4k
views
Comment:
C: Ancestry Informative Markers
7.5 years ago by
stolarek.ir
▴ 700
2
votes
1
reply
2.4k
views
Comment:
C: Ancestry Informative Markers
7.5 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
2.0k
views
Comment:
C: Difference between PATRIC's WGS and COMPLETE genomes
7.6 years ago by
stolarek.ir
▴ 700
1
vote
0
replies
4.6k
views
Comment:
C: bwa mem misaligns my contigs to the reference by a few bases
7.6 years ago by
stolarek.ir
▴ 700
1
vote
1
reply
4.6k
views
Comment:
C: bwa mem misaligns my contigs to the reference by a few bases
7.6 years ago by
stolarek.ir
▴ 700
0
votes
0
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4.0k
views
Comment:
C: How to interpret genotypes with DP=1 for a vcf file
7.8 years ago by
stolarek.ir
▴ 700
2
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0
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2.4k
views
Comment:
C: How to understand likelihood ratio (LR) in GWAS?
7.8 years ago by
stolarek.ir
▴ 700
0
votes
0
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1.9k
views
Comment:
C: Calculating LD between specific alleles even if they are not the minor alleles
7.9 years ago by
stolarek.ir
▴ 700
0
votes
0
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9.7k
views
Comment:
C: Samtools consensus sequence
7.9 years ago by
stolarek.ir
▴ 700
0
votes
0
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4.4k
views
Comment:
C: Different alignments rates with bwa mem (0%) and bowtie2 (82%)
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
8.0k
views
Comment:
C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
8.0 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
8.0k
views
Comment:
C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
8.0k
views
Comment:
C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
8.0 years ago by
stolarek.ir
▴ 700
1
vote
1
reply
8.0k
views
Comment:
C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
8.0 years ago by
stolarek.ir
▴ 700
1
vote
0
replies
1.9k
views
Comment:
C: Estimate signifiant loci in GWAS
8.0 years ago by
stolarek.ir
▴ 700
1
vote
0
replies
2.6k
views
Comment:
C: Reproductivity of publicly available reads
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
7.2k
views
Comment:
C: How to "haploidize" diploid SNPs data in a vcf file
8.0 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
2.6k
views
Comment:
C: Reproductivity of publicly available reads
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
2.4k
views
Comment:
C: Converting .sam to .bam with samtools and I get a new error with every repeated
8.0 years ago by
stolarek.ir
▴ 700
2
votes
0
replies
2.6k
views
Comment:
C: Reproductivity of publicly available reads
8.0 years ago by
stolarek.ir
▴ 700
1
vote
0
replies
1.8k
views
Comment:
C: Profile of methylation about the centromeres/telomeres of human
8.0 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
5.9k
views
Comment:
C: Antisense transcription - how to detect it?
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
2.4k
views
Comment:
C: Conversion of genotype data: GEN format to matrix with genotypes encoded as 0, 1
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
2.4k
views
Comment:
C: How to do clustering of bacteria genome based on hamming distance.
8.0 years ago by
stolarek.ir
▴ 700
1
vote
1
reply
4.0k
views
Comment:
C: What's a good PacBio CLR read simulator?
8.0 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
3.0k
views
Comment:
C: plink PED file - randomly select allele at heterozygous site and convert to homo
8.2 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
3.0k
views
Comment:
C: plink PED file - randomly select allele at heterozygous site and convert to homo
8.2 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
14k
views
Comment:
C: GC content calculation
8.2 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
2.1k
views
Comment:
C: 1000 genomes, meaning of the color of pie charts for population genetic
8.2 years ago by
stolarek.ir
▴ 700
0
votes
1
reply
3.9k
views
Comment:
C: How To Get Chromosome Position Given Rs Number?
8.2 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
2.9k
views
Comment:
C: Removing duplicates in high coverage ancient DNA mitochondrial data
8.4 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
2.9k
views
Comment:
C: Removing duplicates in high coverage ancient DNA mitochondrial data
8.4 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
7.4k
views
Comment:
C: Error while trying to get consensus Fastq from BAM
8.9 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
44k
views
Comment:
C: Extract subset of samples from multigenome vcf file
8.9 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
1.8k
views
Comment:
C: Select one allele at heterozygote position
8.9 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
1.8k
views
Comment:
C: Select one allele at heterozygote position
updated 8.9 years ago by
Pierre Lindenbaum
165k • written 8.9 years ago by
stolarek.ir
▴ 700
2
votes
1
reply
7.9k
views
Comment:
C: minor allele frequency (MAF) from vcf
8.9 years ago by
stolarek.ir
▴ 700
4
votes
0
replies
6.3k
views
Comment:
C: Split Reads vs Supplementary Reads
8.9 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
5.8k
views
Comment:
C: How to properly merge data with 1000 Genomes data for PCA
8.9 years ago by
stolarek.ir
▴ 700
0
votes
0
replies
1.9k
views
Comment:
C: SNPs in samtools mpileup using multisample and individual samples
9.0 years ago by
stolarek.ir
▴ 700
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