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Answer: C: SNPs data in genomic sequences
updated 5.7 years ago by 45k • written 10.6 years ago by ▴ 420
1
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1
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7.8k
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Answer: Answer: VCFtools LD calculations only for pairs that include a single SNP of interest
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
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Comment: C: GGplot adding scales under specific graphs.
10.2 years ago by smilefreak ▴ 420
7
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3
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GGplot adding scales under specific graphs.
ggplot2 R NGS
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 420
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1
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1.5k
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Resequencing region selection
EXOME NGS
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 420
10
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2
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6.0k
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BWA MEM and ancient DNA
alignment aDNA
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
6
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1
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6.8k
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Comment: C: Are we seeing a bioinformatician shortage?
10.6 years ago by smilefreak ▴ 420
0
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3.6k
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Comment: Comment: What is reciprocal partners?
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
1
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1
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3.6k
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Comment: Comment: What is reciprocal partners?
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
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2.0k
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Comment: C: RNAseq Read length distribution FFPE
10.6 years ago by smilefreak ▴ 420
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7.7k
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Comment: Comment: Problem is to design model matrix for edgeR
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
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3.3k
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Answer: Answer: subset fastq file
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
0
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1
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7.8k
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Comment: Comment: Split a concatenated alignment into individual gene alignments
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
0
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1
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7.8k
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Comment: Comment: Split a concatenated alignment into individual gene alignments
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
0
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1
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7.8k
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Comment: Comment: Split a concatenated alignment into individual gene alignments
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
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0
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4.5k
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Answer: Answer: Simple shell command for extracting indexed reads from fastq?
updated 4.2 years ago by 45k • written 10.6 years ago by ▴ 420
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6.9k
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Comment: Comment: Detecting selection with 'selscan' - How can I generate the correct input files
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
0
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1
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6.9k
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Comment: Comment: Detecting selection with 'selscan' - How can I generate the correct input files
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
0
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1
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3.6k
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Comment: Comment: SIFT ncbi executables setup incorrectly?
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
3
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2
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3.6k
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Answer: Answer: SIFT ncbi executables setup incorrectly?
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
3
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0
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4.4k
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Answer: Answer: How to group genes as 'gene sets'
updated 4.2 years ago by 45k • written 10.6 years ago by ▴ 420
3
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0
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5.3k
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Answer: Answer: CIGAR M operator maps off end of reference
updated 4.2 years ago by 45k • written 10.6 years ago by ▴ 420
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0
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1.7k
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Comment: Comment: more contigs of different samples to a gene fragment
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 420
1
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1
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52k
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Answer: Answer: Fastq Splitter For Paired End Reads
updated 4.2 years ago by 45k • written 10.6 years ago by ▴ 420
0
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1
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2.7k
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Comment: Comment: finding co-expression genes
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
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2.7k
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Comment: Comment: finding co-expression genes
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
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0
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6.2k
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Comment: Comment: Barcode (index) splitting
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
1
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0
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2.2k
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Answer: Answer: Getting Haplotype data from 1000 genome project
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
0
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0
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7.8k
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Comment: Comment: VCFtools LD calculations only for pairs that include a single SNP of interest
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
3
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0
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3.2k
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Answer: Answer: How to get list of 150 bp sequences for each of 15,000 from chromosome positions
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
0
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1
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10.0k
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Answer: Answer: How to draw Chow-Ruskey diagram (more than 6 elements) with Vennerable R package
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
1
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0
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4.1k
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Comment: Comment: Public Disease Exomes (VCF)
updated 3.4 years ago by 45k • written 10.7 years ago by ▴ 420
0
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0
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5.0k
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Comment: C: How to start CNV analysis via Plink?
10.7 years ago by smilefreak ▴ 420
1
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1
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4.0k
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Comment: Comment: How to reduce the number of SNPs for the Lositan software
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
0
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0
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2.3k
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Comment: Comment: How to interpate information of fastq formate read files ?
updated 3.4 years ago by 45k • written 10.7 years ago by ▴ 420
0
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0
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2.1k
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Answer: Answer: Significantly mutated genes without control
updated 3.4 years ago by 45k • written 10.7 years ago by ▴ 420
1
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0
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2.4k
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Comment: C: Using GRCH37 with ggbio
updated 4.2 years ago by 45k • written 10.7 years ago by ▴ 420
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