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1
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3.3k
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Comment: C: Does BWA mem ever edit data
6.4 years ago by dariober 15k
3
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2.1k
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Answer: A: script for task or AWK
6.4 years ago by dariober 15k
2
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5.1k
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Answer: A: How to assess the Fold-change significance using a t-test in R?
6.4 years ago by dariober 15k
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3.0k
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Comment: C: Installing IGV on Bio-linux 8 - Installing All Dependancies At Once
6.4 years ago by dariober 15k
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3.0k
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Answer: A: Installing IGV on Bio-linux 8 - Installing All Dependancies At Once
6.4 years ago by dariober 15k
7
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1
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7.2k
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Answer: A: Picard liftoverVCF error when attempting to liftover to build 38
6.4 years ago by dariober 15k
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4.2k
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Answer: A: What is the computation requirement to process whole genome paired end data each
6.4 years ago by dariober 15k
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1
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1.5k
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Comment: C: statistics data, observed vs expected values
6.5 years ago by dariober 15k
1
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1
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1.8k
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Answer: A: How can I compute if the co-occurrence of two TFBSs within a certain width in al
6.5 years ago by dariober 15k
1
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1
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4.9k
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Answer: A: Bimodal p-value distribution
6.5 years ago by dariober 15k
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2
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2.5k
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Comment: C: Where can I download homo sapiens gene locations file including ensembl gene id,
6.5 years ago by dariober 15k
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2.5k
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Comment: C: Where can I download homo sapiens gene locations file including ensembl gene id,
6.5 years ago by dariober 15k
1
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2
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1.8k
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Comment: C: Variant with AD 14,3 is heterozygote?
6.5 years ago by dariober 15k
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1
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1.6k
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Answer: A: GATK gradlew bundle Error
6.5 years ago by dariober 15k
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0
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1.9k
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Answer: A: bwa mem without -M option how to continue using picard
6.6 years ago by dariober 15k
0
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1
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2.1k
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Comment: C: What are the methods to downsample the Depth of coverage (ex: 50X -> 25X)?
6.6 years ago by dariober 15k
3
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1
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2.9k
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Answer: A: Where can I find GV .genome files for igvtools
6.6 years ago by dariober 15k
1
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1
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3.2k
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Answer: A: Overlap of variants between CaVEMan and MuTect2 ?
6.6 years ago by dariober 15k
0
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0
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1.9k
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Answer: A: Is there an available tool to visualize multiple "types" of ChIP-seq peaks on a
6.6 years ago by dariober 15k
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2
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4.0k
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Comment: C: How to get a matrix gene weights in NMF
6.6 years ago by dariober 15k
3
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1
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4.0k
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Answer: A: How to get a matrix gene weights in NMF
6.6 years ago by dariober 15k
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0
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4.3k
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Answer: A: Why IVG coverage track from bam and bigwig files looks different?
6.6 years ago by dariober 15k
1
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0
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4.9k
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Answer: A: How to generate random genomic sequences that are GC- and length-matched to my i
6.6 years ago by dariober 15k
3
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0
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1.9k
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Comment: C: How to check if a read in a SAM file contains substitutions
6.6 years ago by dariober 15k
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2
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19k
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Answer: A: bwa mem and multiply mapped reads
6.6 years ago by dariober 15k
1
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1
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2.5k
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Answer: A: Why different DEGs between my result and the author's result?
6.6 years ago by dariober 15k
4
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0
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7.0k
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Answer: A: Interesting/useful/beautiful bio sequence viz tools
6.6 years ago by dariober 15k
2
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1
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3.0k
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Answer: A: dbSNP Batch Query service will be discontinued June 2018: alternatives?
6.6 years ago by dariober 15k
1
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1
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1.8k
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Answer: A: Finding all possible alignments of two sequences
6.6 years ago by dariober 15k
1
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0
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7.0k
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Answer: A: Is there a better tool for visualizing your variants after annotation than Excel
6.6 years ago by dariober 15k
3
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0
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7.0k
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Answer: A: Is there a better tool for visualizing your variants after annotation than Excel
6.7 years ago by dariober 15k
0
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1
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4.8k
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Comment: C: SAM MD tag for consecutive insertions/deletions
6.7 years ago by dariober 15k
0
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1
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4.8k
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Answer: A: SAM MD tag for consecutive insertions/deletions
6.7 years ago by dariober 15k
0
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1
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5.8k
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Comment: C: intersection, Bed file and VCF.
6.7 years ago by dariober 15k
0
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1
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5.8k
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Answer: A: intersection, Bed file and VCF.
6.7 years ago by dariober 15k
1
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0
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1.8k
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Answer: A: Categorize patients based on continuous variables
6.7 years ago by dariober 15k
2
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1
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1.9k
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Answer: A: Removing spike-in sequences from oxidative bisulfite (OXBS) fastq files
6.7 years ago by dariober 15k
3
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0
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1.4k
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Answer: A: Tools to assess coverage and error rate at specific position
6.7 years ago by dariober 15k
0
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0
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11k
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Answer: A: IGV command line control
6.7 years ago by dariober 15k
2
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0
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3.5k
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Answer: A: How to get the coordinations of CpG sites in non-human genome
6.7 years ago by dariober 15k
3
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1
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12k
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Comment: C: TMB Tumor Mutation Burden
6.7 years ago by dariober 15k
1
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0
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1.7k
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Comment: C: Sorting file by column, with missing values
6.7 years ago by dariober 15k
2
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0
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3.1k
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Answer: A: Plotting common SNPs from four individual from a vcf file
6.7 years ago by dariober 15k
2
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1
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2.3k
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Answer: A: MuTect2 still discard many reads, how to fix?
6.7 years ago by dariober 15k
3
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0
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3.9k
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Answer: A: Ideas to plot several enrichment results (BP) in one
6.7 years ago by dariober 15k
0
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1
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3.2k
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Comment: C: WGS data for pipeline development
6.7 years ago by dariober 15k
1
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1
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2.9k
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Comment: C: Importing Uniprot into BioSQL using BioPython takes years (nearly literally!)
6.7 years ago by dariober 15k
2
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0
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2.9k
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Comment: C: Importing Uniprot into BioSQL using BioPython takes years (nearly literally!)
6.7 years ago by dariober 15k
1
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1
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4.0k
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Answer: A: CosmicCodingMuts.vcf.gz for hg38?
6.7 years ago by dariober 15k
0
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0
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2.7k
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Answer: A: R books with Quantitative Genetics examples?
6.7 years ago by dariober 15k
1,134 results • Page 10 of 23
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