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37
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8
replies
51k
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Adding Read Groups To Bam Files
bam gatk samtools bwa
updated 2.9 years ago by 11k • written 11.8 years ago by 12k
0
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1
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25k
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Comment: A: Extract Base Based On Position From Bam File
updated 3.7 years ago by 43k • written 11.8 years ago by 12k
2
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3
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1.4k
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building all possible phylogenies.
phylogenetics
updated 3.8 years ago by 20 • written 7.1 years ago by 12k
0
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1
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59k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 3.9 years ago by 43k • written 11.7 years ago by 12k
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0
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59k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 3.9 years ago by 43k • written 9.4 years ago by 12k
11
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1
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59k
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Answer: A: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 3.9 years ago by 43k • written 12.0 years ago by 12k
4
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0
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4.2k
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Answer: A: Per Base Coverage
updated 4.1 years ago by 43k • written 12.1 years ago by 12k
5
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1
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5.1k
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Answer: A: Fast kmer reverse complement code using bit tricks
4.2 years ago by Zev.Kronenberg 12k
1
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0
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5.1k
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Comment: C: Fast kmer reverse complement code using bit tricks
4.2 years ago by Zev.Kronenberg 12k
1
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1
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12k
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Comment: C: how to get the genotypes from vcf file.
updated 4.3 years ago by 43k • written 8.2 years ago by 12k
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2
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15k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 4.3 years ago by 43k • written 8.2 years ago by 12k
0
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1
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2.5k
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Comment: C: Linkage Disequlibirum (R^2) = recombination?
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
1
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2
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2.2k
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Answer: A: Exome sequencing ?
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
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0
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1.9k
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Comment: C: Make figures for SNP detected
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
1
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0
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1.7k
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Answer: A: Building a reference genome for pop differentiation.
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
0
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1
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5.7k
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Comment: C: Software for Mcdonald-Kreitman test
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
0
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1
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4.0k
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Answer: A: FST: allele-counts or allele-frequencies?
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
3
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1
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10k
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Comment: C: Is it worth getting a Masters in Bioinformatics, financially?
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
3
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2
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16k
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Answer: A: R: Manhattan Plot Of Fst Values Instead Of -Log(P)
updated 4.3 years ago by 43k • written 12.1 years ago by 12k
0
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1
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16k
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Comment: C: R: Manhattan Plot Of Fst Values Instead Of -Log(P)
updated 4.3 years ago by 43k • written 10.8 years ago by 12k
0
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0
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16k
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Comment: C: R: Manhattan Plot Of Fst Values Instead Of -Log(P)
updated 4.3 years ago by 43k • written 9.4 years ago by 12k
4
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0
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9.1k
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Answer: A: Summarising Whole Genome Allele Frequency Spectrum from VCF file
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
2
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1
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9.1k
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Answer: A: Summarising Whole Genome Allele Frequency Spectrum from VCF file
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
0
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0
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8.1k
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Answer: A: Phred quality Score
updated 4.3 years ago by 43k • written 9.9 years ago by 12k
2
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1
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2.5k
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Answer: A: Background information and recommendations for phasing ASW whole genomes
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
0
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1
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3.3k
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Comment: C: how to compare the Ka/Ks ratio for chromosomes
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
0
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1
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8.6k
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Comment: C: Programs to View MrBayes Consensus Trees
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
0
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0
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1.7k
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Comment: C: VCFclin working group
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
0
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1
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8.6k
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Comment: C: Programs to View MrBayes Consensus Trees
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
1
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1
reply
8.6k
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Answer: A: Programs to View MrBayes Consensus Trees
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
1
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0
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2.7k
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Comment: C: Circos: can it be used with gene expression data and Orbitrap/Kinexus data?
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
0
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1
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4.4k
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Answer: A: Interpreting XPEHH output
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
0
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0
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5.7k
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Comment: C: Linkage information from unphased VCF files
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
3
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1
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5.7k
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Answer: A: Linkage information from unphased VCF files
updated 4.3 years ago by 43k • written 10.0 years ago by 12k
2
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0
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10k
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Comment: C: dxy (Nei 1987) calculation
updated 4.3 years ago by 43k • written 8.3 years ago by 12k
2
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0
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1.8k
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Answer: A: finding gene variation using Fasta files
updated 4.3 years ago by 43k • written 8.3 years ago by 12k
4
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1
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7.7k
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Answer: A: Are XA: tagged reads == SA: tagged BWAMEM aligned reads?
updated 4.4 years ago by 43k • written 8.4 years ago by 12k
0
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0
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8.0k
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Answer: Answer: Finding gene density from reference genome using R
updated 4.4 years ago by 43k • written 8.4 years ago by 12k
2
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1
reply
14k
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Answer: A: Dp And Dp4 In Vcf
updated 4.4 years ago by 43k • written 11.9 years ago by 12k
1
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0
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2.2k
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Comment: C: Phasing a portion of chromosome vs whole chromosome using Beagle?
updated 4.4 years ago by 43k • written 8.4 years ago by 12k
0
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4
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24k
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Answer: A: How To Construct Phylogenetic Tree Using Snps
updated 4.4 years ago by 43k • written 12.2 years ago by 12k
0
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1
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15k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 4.4 years ago by 43k • written 8.5 years ago by 12k
0
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0
replies
15k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 4.4 years ago by 43k • written 8.5 years ago by 12k
0
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1
reply
4.7k
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Comment: C: VCFtools LD for haploids is nan
updated 4.4 years ago by 43k • written 8.5 years ago by 12k
1
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1
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4.7k
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Answer: A: VCFtools LD for haploids is nan
updated 4.4 years ago by 43k • written 8.5 years ago by 12k
0
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1
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15k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 4.4 years ago by 43k • written 8.5 years ago by 12k
1
vote
1
reply
15k
views
Answer: A: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 4.4 years ago by 43k • written 8.5 years ago by 12k
2
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4
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18k
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Answer: A: ADMIXTURE and R, color meaning on barplot in studing population ancestry, K valu
updated 4.4 years ago by 43k • written 8.6 years ago by 12k
0
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0
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1.7k
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Comment: C: Genotyping CNVs from Next Generation Sequencing data
updated 4.4 years ago by 43k • written 8.6 years ago by 12k
1
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1
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1.7k
views
Answer: A: Genotyping CNVs from Next Generation Sequencing data
updated 4.4 years ago by 43k • written 8.6 years ago by 12k
926 results • Page 1 of 19
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