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37
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8
replies
53k
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Adding Read Groups To Bam Files
bam gatk samtools bwa
updated 3.4 years ago by 12k • written 12.4 years ago by 12k
0
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1
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27k
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Comment: A: Extract Base Based On Position From Bam File
updated 4.2 years ago by 44k • written 12.4 years ago by 12k
2
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3
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1.5k
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building all possible phylogenies.
phylogenetics
updated 4.4 years ago by 20 • written 7.6 years ago by 12k
0
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1
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66k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.5 years ago by 44k • written 12.3 years ago by 12k
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0
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66k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.5 years ago by 44k • written 10.0 years ago by 12k
11
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1
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66k
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Answer: A: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.5 years ago by 44k • written 12.6 years ago by 12k
4
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0
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4.3k
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Answer: A: Per Base Coverage
updated 4.7 years ago by 44k • written 12.7 years ago by 12k
5
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1
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5.5k
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Answer: A: Fast kmer reverse complement code using bit tricks
4.7 years ago by Zev.Kronenberg 12k
1
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0
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5.5k
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Comment: C: Fast kmer reverse complement code using bit tricks
4.7 years ago by Zev.Kronenberg 12k
1
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1
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13k
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Comment: C: how to get the genotypes from vcf file.
updated 4.9 years ago by 44k • written 8.8 years ago by 12k
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2
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16k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 4.9 years ago by 44k • written 8.8 years ago by 12k
0
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1
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2.6k
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Comment: C: Linkage Disequlibirum (R^2) = recombination?
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
1
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2
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2.3k
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Answer: A: Exome sequencing ?
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
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0
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2.0k
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Comment: C: Make figures for SNP detected
updated 4.9 years ago by 44k • written 10.5 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 4.9 years ago by 44k • written 10.5 years ago by 12k
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1
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6.1k
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Comment: C: Software for Mcdonald-Kreitman test
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
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1
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4.2k
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Answer: A: FST: allele-counts or allele-frequencies?
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
3
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1
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11k
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Comment: C: Is it worth getting a Masters in Bioinformatics, financially?
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
3
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2
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17k
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Answer: A: R: Manhattan Plot Of Fst Values Instead Of -Log(P)
updated 4.9 years ago by 44k • written 12.7 years ago by 12k
0
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1
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17k
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Comment: C: R: Manhattan Plot Of Fst Values Instead Of -Log(P)
updated 4.9 years ago by 44k • written 11.4 years ago by 12k
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0
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17k
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Comment: C: R: Manhattan Plot Of Fst Values Instead Of -Log(P)
updated 4.9 years ago by 44k • written 10.0 years ago by 12k
4
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0
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9.4k
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Answer: A: Summarising Whole Genome Allele Frequency Spectrum from VCF file
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
2
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1
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9.4k
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Answer: A: Summarising Whole Genome Allele Frequency Spectrum from VCF file
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
0
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0
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8.4k
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Answer: A: Phred quality Score
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
2
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1
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2.6k
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Answer: A: Background information and recommendations for phasing ASW whole genomes
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
0
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1
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3.5k
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Comment: C: how to compare the Ka/Ks ratio for chromosomes
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
0
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1
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8.9k
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Comment: C: Programs to View MrBayes Consensus Trees
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
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0
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1.9k
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Comment: C: VCFclin working group
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
0
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1
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8.9k
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Comment: C: Programs to View MrBayes Consensus Trees
updated 4.9 years ago by 44k • written 10.5 years ago by 12k
1
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1
reply
8.9k
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Answer: A: Programs to View MrBayes Consensus Trees
updated 4.9 years ago by 44k • written 10.6 years ago by 12k
1
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0
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2.8k
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Comment: C: Circos: can it be used with gene expression data and Orbitrap/Kinexus data?
updated 4.9 years ago by 44k • written 10.6 years ago by 12k
0
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1
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4.7k
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Answer: A: Interpreting XPEHH output
updated 4.9 years ago by 44k • written 10.6 years ago by 12k
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0
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6.0k
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Comment: C: Linkage information from unphased VCF files
updated 4.9 years ago by 44k • written 10.6 years ago by 12k
3
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1
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6.0k
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Answer: A: Linkage information from unphased VCF files
updated 4.9 years ago by 44k • written 10.6 years ago by 12k
2
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0
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11k
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Comment: C: dxy (Nei 1987) calculation
updated 4.9 years ago by 44k • written 8.8 years ago by 12k
2
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0
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1.9k
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Answer: A: finding gene variation using Fasta files
updated 4.9 years ago by 44k • written 8.9 years ago by 12k
4
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1
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8.4k
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Answer: A: Are XA: tagged reads == SA: tagged BWAMEM aligned reads?
updated 4.9 years ago by 44k • written 8.9 years ago by 12k
0
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0
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8.5k
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Answer: Answer: Finding gene density from reference genome using R
updated 4.9 years ago by 44k • written 9.0 years ago by 12k
2
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1
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14k
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Answer: A: Dp And Dp4 In Vcf
updated 5.0 years ago by 44k • written 12.5 years ago by 12k
1
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0
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2.3k
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Comment: C: Phasing a portion of chromosome vs whole chromosome using Beagle?
updated 5.0 years ago by 44k • written 9.0 years ago by 12k
0
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4
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25k
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Answer: A: How To Construct Phylogenetic Tree Using Snps
updated 5.0 years ago by 44k • written 12.8 years ago by 12k
0
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1
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16k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 5.0 years ago by 44k • written 9.1 years ago by 12k
0
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0
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16k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 5.0 years ago by 44k • written 9.1 years ago by 12k
0
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1
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5.0k
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Comment: C: VCFtools LD for haploids is nan
updated 5.0 years ago by 44k • written 9.1 years ago by 12k
1
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1
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5.0k
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Answer: A: VCFtools LD for haploids is nan
updated 5.0 years ago by 44k • written 9.1 years ago by 12k
0
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1
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16k
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Comment: C: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 5.0 years ago by 44k • written 9.1 years ago by 12k
1
vote
1
reply
16k
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Answer: A: A Database Of Signatures Of Selection In The 1000 Genomes Dataset
updated 5.0 years ago by 44k • written 9.1 years ago by 12k
2
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4
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19k
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Answer: A: ADMIXTURE and R, color meaning on barplot in studing population ancestry, K valu
updated 5.0 years ago by 44k • written 9.2 years ago by 12k
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0
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1.9k
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Comment: C: Genotyping CNVs from Next Generation Sequencing data
updated 5.0 years ago by 44k • written 9.2 years ago by 12k
1
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1
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1.9k
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Answer: A: Genotyping CNVs from Next Generation Sequencing data
updated 5.0 years ago by 44k • written 9.2 years ago by 12k
926 results • Page 1 of 19
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