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Comment: C: 1000 genomes, meaning of the color of pie charts for population genetic
7.0 years ago by stolarek.ir ▴ 700
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1
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3.5k
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Comment: C: How To Get Chromosome Position Given Rs Number?
7.0 years ago by stolarek.ir ▴ 700
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2.3k
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Comment: C: Removing duplicates in high coverage ancient DNA mitochondrial data
7.2 years ago by stolarek.ir ▴ 700
3
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6
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2.3k
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Removing duplicates in high coverage ancient DNA mitochondrial data
aDNA duplicates Picard
updated 7.2 years ago by ★ 3.8k • written 7.2 years ago by ▴ 700
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2.3k
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Comment: C: Removing duplicates in high coverage ancient DNA mitochondrial data
7.2 years ago by stolarek.ir ▴ 700
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3
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1.6k
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Select one allele at heterozygote position
SNP vcf plink
updated 7.6 years ago by 20 • written 7.7 years ago by ▴ 700
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6.7k
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Comment: C: Error while trying to get consensus Fastq from BAM
7.7 years ago by stolarek.ir ▴ 700
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38k
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Comment: C: Extract subset of samples from multigenome vcf file
7.7 years ago by stolarek.ir ▴ 700
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1.6k
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Comment: C: Select one allele at heterozygote position
7.7 years ago by stolarek.ir ▴ 700
0
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0
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1.6k
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Comment: C: Select one allele at heterozygote position
updated 7.7 years ago by 158k • written 7.7 years ago by ▴ 700
2
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1
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7.3k
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Comment: C: minor allele frequency (MAF) from vcf
7.7 years ago by stolarek.ir ▴ 700
4
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6.0k
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Comment: C: Split Reads vs Supplementary Reads
7.7 years ago by stolarek.ir ▴ 700
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0
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5.1k
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Comment: C: How to properly merge data with 1000 Genomes data for PCA
7.7 years ago by stolarek.ir ▴ 700
4
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1
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8.9k
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Answer: A: Samtools consensus sequence
updated 7.7 years ago by 99k • written 7.7 years ago by ▴ 700
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1.9k
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Answer: A: Are these reads all PCR replicates ?
7.7 years ago by stolarek.ir ▴ 700
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1.7k
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Comment: C: SNPs in samtools mpileup using multisample and individual samples
7.7 years ago by stolarek.ir ▴ 700
0
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1
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5.1k
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Comment: C: How to properly merge data with 1000 Genomes data for PCA
7.7 years ago by stolarek.ir ▴ 700
0
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0
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2.8k
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Comment: C: Find all SNPs in linkage disequilibrium
7.7 years ago by stolarek.ir ▴ 700
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0
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2.7k
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Answer: A: How to identify the ancestral population to which an individual belongs knowing
7.7 years ago by stolarek.ir ▴ 700
2
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0
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4.9k
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Comment: C: PhD research proposal - Need current topics
7.8 years ago by stolarek.ir ▴ 700
0
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1
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2.0k
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Comment: C: SmartPCA gives very different PCs for different chromosomes
7.9 years ago by stolarek.ir ▴ 700
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7.1k
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Comment: C: Intersect multiple BED files
7.9 years ago by stolarek.ir ▴ 700
0
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1
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4.0k
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Comment: C: F3 test for admixture
8.0 years ago by stolarek.ir ▴ 700
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4.1k
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Comment: C: Calculate Allele Frequency from PLINK PED/MAP files
8.1 years ago by stolarek.ir ▴ 700
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0
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6.1k
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Comment: C: SNP and gene density along the chromosomes plots
8.1 years ago by stolarek.ir ▴ 700
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0
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3.1k
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Comment: C: FASTAQ to BAM
8.1 years ago by stolarek.ir ▴ 700
2
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1.6k
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Comment: C: Bioinformatics for a Information Systems graduate?
8.1 years ago by stolarek.ir ▴ 700
0
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0
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1.7k
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Comment: Comment: Data for Pairwise Sequence Alignment
updated 15 months ago by 41k • written 8.1 years ago by ▴ 700
1
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0
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1.6k
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Comment: C: SNP Data from dbSNP
8.1 years ago by stolarek.ir ▴ 700
0
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1
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3.6k
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Comment: C: regarding to Fastqc and SRA file format
8.1 years ago by stolarek.ir ▴ 700
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0
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2.1k
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Comment: C: Help in identifying quality from FASTQC on illumina RNA sequences
8.1 years ago by stolarek.ir ▴ 700
0
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0
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3.1k
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Comment: Comment: Efficient means of mass converting Affy SNP IDs to dbSNP rs ids
updated 10 months ago by 41k • written 8.1 years ago by ▴ 700
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4.4k
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Comment: C: Should I use Illumina or Ion Torrent for producing data intended for genome rese
8.1 years ago by stolarek.ir ▴ 700
1
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1
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3.4k
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Comment: C: How to merge VCF files for SNP's ?
8.1 years ago by stolarek.ir ▴ 700
1
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0
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4.8k
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Comment: C: How can I deal with adapter contamination in next-gen sequencing reads?
8.1 years ago by stolarek.ir ▴ 700
1
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1
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9.3k
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Comment: C: Convert Tab delimited file to VCF file
8.1 years ago by stolarek.ir ▴ 700
1
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1
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2.1k
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Answer: A: alignments of DNA sequences
8.1 years ago by stolarek.ir ▴ 700
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2
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2.1k
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Answer: A: Help in identifying quality from FASTQC on illumina RNA sequences
8.1 years ago by stolarek.ir ▴ 700
1
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0
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4.0k
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plink 1.9 PED to VCF, SNPs differ on input and output files
plink SNP
updated 14 months ago by 41k • written 8.2 years ago by ▴ 700
5
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1
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3.0k
views
Hash Table Vs Suffix Array Alignment Error Tolerance
bwa
updated 13 months ago by 41k • written 9.7 years ago by ▴ 700
0
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0
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1.9k
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Comment: Comment: Determine number of regions, that weren't capture during shallow NGS sequencing
updated 10 months ago by 41k • written 8.5 years ago by ▴ 700
1
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2
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1.9k
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Determine number of regions, that weren't capture during shallow NGS sequencing
snp aDNA next-gen-sequencing
updated 10 months ago by 41k • written 8.5 years ago by ▴ 700
0
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1
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4.7k
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Answer: A: metagenomics of gut sequences
8.5 years ago by stolarek.ir ▴ 700
1
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0
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3.9k
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Answer: Answer: IGV and Variant Call
updated 10 months ago by 41k • written 8.5 years ago by ▴ 700
0
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5
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2.3k
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Missing Cigar In Sam Output (Cushaw2)
sam cigar
updated 9.5 years ago by 20 • written 10.0 years ago by ▴ 700
0
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0
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3.4k
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Mpileup Problem
mpileup vcf samtools
updated 9.8 years ago by 20 • written 10.3 years ago by ▴ 700
0
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1
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1.7k
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Simulate Genome Fasta With Indels
9.9 years ago by stolarek.ir ▴ 700
0
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1
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2.3k
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Comment: C: Missing Cigar In Sam Output (Cushaw2)
10.0 years ago by stolarek.ir ▴ 700
0
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0
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2.3k
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Comment: C: Missing Cigar In Sam Output (Cushaw2)
10.0 years ago by stolarek.ir ▴ 700
0
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0
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3.3k
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Comment: C: Bwa Soft Clipped Indels Realignment
10.2 years ago by stolarek.ir ▴ 700
122 results • Page 2 of 3
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