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432
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Answer: Answer: Align concatameric reads to region
20 months ago by stolarek.ir ▴ 700
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818
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Comment: Comment: gtf2bed doesn't give gene_id in the bed file
20 months ago by stolarek.ir ▴ 700
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1.0k
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Answer: Answer: strand specific data
20 months ago by stolarek.ir ▴ 700
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7.7k
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Answer: A: Intersect multiple BED files
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 700
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2.4k
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Comment: C: How I can reduce the depth of a sequencing when I want to assemble it?
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 700
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4.9k
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Comment: C: Heatmap of Differentially Expressed Genes
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 700
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0
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6.2k
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Comment: C: How to convert Affymetrix SNP IDs to dbSNP rs SNP names
updated 4.4 years ago by 43k • written 8.5 years ago by ▴ 700
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1
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771
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PacBio base modifications merging p6c2 and p4c2
PacBio base modifications
updated 5.1 years ago by ▴ 20 • written 5.1 years ago by ▴ 700
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5.5k
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Comment: C: Merging files in plink
6.1 years ago by stolarek.ir ▴ 700
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2.7k
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Answer: A: ABBA-BABA D statistics to pattern introgressed loci: applicable to RNA-seq data?
6.1 years ago by stolarek.ir ▴ 700
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0
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4.1k
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Answer: A: STAR analysis and alignment
6.2 years ago by stolarek.ir ▴ 700
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1
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3.1k
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Comment: C: Illumina paired end read header difference- SPAdes bwa run ERROR
6.6 years ago by stolarek.ir ▴ 700
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0
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3.2k
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Comment: C: RNASeq lane effect
6.6 years ago by stolarek.ir ▴ 700
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1
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4.7k
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Comment: C: long reads Pacbio SNP calling
6.6 years ago by stolarek.ir ▴ 700
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1
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4.7k
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Answer: A: long reads Pacbio SNP calling
6.6 years ago by stolarek.ir ▴ 700
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1.7k
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codeml, output tree topology different from the input tree
codeml paml
6.6 years ago by stolarek.ir ▴ 700
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0
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12k
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Comment: C: Paired vs unpaired (DNA Sequencing)
6.7 years ago by stolarek.ir ▴ 700
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1
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2.1k
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Comment: C: How to align multiple genomic regions simultaneously
6.7 years ago by stolarek.ir ▴ 700
2
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4.4k
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Answer: A: PLINK RECODING ISSUE
6.7 years ago by stolarek.ir ▴ 700
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1
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2.1k
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Comment: C: Ancestry Informative Markers
6.7 years ago by stolarek.ir ▴ 700
2
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1
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2.1k
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Comment: C: Ancestry Informative Markers
6.7 years ago by stolarek.ir ▴ 700
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1
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1.8k
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Comment: C: Difference between PATRIC's WGS and COMPLETE genomes
6.8 years ago by stolarek.ir ▴ 700
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0
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4.0k
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Comment: C: bwa mem misaligns my contigs to the reference by a few bases
6.8 years ago by stolarek.ir ▴ 700
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1
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4.0k
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Comment: C: bwa mem misaligns my contigs to the reference by a few bases
6.8 years ago by stolarek.ir ▴ 700
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0
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3.7k
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Comment: C: How to interpret genotypes with DP=1 for a vcf file
7.0 years ago by stolarek.ir ▴ 700
2
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0
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2.2k
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Comment: C: How to understand likelihood ratio (LR) in GWAS?
7.0 years ago by stolarek.ir ▴ 700
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0
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1.7k
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Comment: C: Calculating LD between specific alleles even if they are not the minor alleles
7.1 years ago by stolarek.ir ▴ 700
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0
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9.2k
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Comment: C: Samtools consensus sequence
7.1 years ago by stolarek.ir ▴ 700
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0
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4.0k
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Comment: C: Different alignments rates with bwa mem (0%) and bowtie2 (82%)
7.2 years ago by stolarek.ir ▴ 700
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0
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7.0k
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Comment: C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
7.2 years ago by stolarek.ir ▴ 700
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1
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7.0k
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Comment: C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
7.2 years ago by stolarek.ir ▴ 700
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0
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7.0k
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Comment: C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
7.2 years ago by stolarek.ir ▴ 700
1
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1
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7.0k
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Comment: C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
7.2 years ago by stolarek.ir ▴ 700
2
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1
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7.0k
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Answer: C: Samtools: merge and mpileup vs mpileup alone for variant-calling with multiple B
7.2 years ago by stolarek.ir ▴ 700
1
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0
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1.7k
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Comment: C: Estimate signifiant loci in GWAS
7.2 years ago by stolarek.ir ▴ 700
1
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0
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2.2k
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Comment: C: Reproductivity of publicly available reads
7.2 years ago by stolarek.ir ▴ 700
0
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0
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6.4k
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Comment: C: How to "haploidize" diploid SNPs data in a vcf file
7.2 years ago by stolarek.ir ▴ 700
0
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1
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2.2k
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Comment: C: Reproductivity of publicly available reads
7.2 years ago by stolarek.ir ▴ 700
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0
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2.2k
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Comment: C: Converting .sam to .bam with samtools and I get a new error with every repeated
7.2 years ago by stolarek.ir ▴ 700
2
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0
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2.2k
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Comment: C: Reproductivity of publicly available reads
7.2 years ago by stolarek.ir ▴ 700
1
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0
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1.6k
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Comment: C: Profile of methylation about the centromeres/telomeres of human
7.2 years ago by stolarek.ir ▴ 700
0
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1
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5.4k
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Comment: C: Antisense transcription - how to detect it?
7.2 years ago by stolarek.ir ▴ 700
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0
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2.2k
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Comment: C: Conversion of genotype data: GEN format to matrix with genotypes encoded as 0, 1
7.2 years ago by stolarek.ir ▴ 700
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0
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2.0k
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Comment: C: How to do clustering of bacteria genome based on hamming distance.
7.2 years ago by stolarek.ir ▴ 700
1
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1
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3.5k
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Comment: C: What's a good PacBio CLR read simulator?
7.2 years ago by stolarek.ir ▴ 700
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0
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2.7k
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Comment: C: plink PED file - randomly select allele at heterozygous site and convert to homo
7.4 years ago by stolarek.ir ▴ 700
0
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0
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2.7k
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Comment: C: plink PED file - randomly select allele at heterozygous site and convert to homo
7.4 years ago by stolarek.ir ▴ 700
2
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3
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2.7k
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plink PED file - randomly select allele at heterozygous site and convert to homozygous
aDNA plink PED SNP Genotype
updated 7.4 years ago by ▴ 10 • written 8.3 years ago by ▴ 700
1
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0
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2.6k
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Answer: A: cd hit for removing sequence redundancy
7.4 years ago by stolarek.ir ▴ 700
0
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0
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12k
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Comment: C: GC content calculation
7.4 years ago by stolarek.ir ▴ 700
122 results • Page 1 of 3
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