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1
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6.1k
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Answer: Answer: filtering the reads based on the length
8 days ago by geocarvalho ▴ 330
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4.6k
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Comment: Comment: filter reads in BAM having a tag
13 days ago by geocarvalho ▴ 330
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2.5k
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Comment: Comment: Paternity Testing from WGS Trio
15 days ago by geocarvalho ▴ 330
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758
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Answer: Answer: Removing multi-variant records from vcf file
19 days ago by geocarvalho ▴ 330
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0
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433
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Answer: Answer: GATK4 ASEReadCounter Function of VCF
19 days ago by geocarvalho ▴ 330
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0
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77k
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Comment: Comment: Extract Sub-Set Of Regions From Vcf File
6 weeks ago by geocarvalho ▴ 330
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4.5k
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Answer: Answer: How to access specifically 30x NA12878 sequencing runs
6 months ago by geocarvalho ▴ 330
1
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0
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890
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Comment: Comment: Understanding bam tracks
8 months ago by geocarvalho ▴ 330
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1
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1.6k
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Comment: Comment: How to retrieve the SNP data from Bam file
16 months ago by geocarvalho ▴ 330
0
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1
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4.2k
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Comment: Comment: Copy Number Variation Tools
16 months ago by geocarvalho ▴ 330
3
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6.3k
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Answer: Answer: snpEFF not able to download GRCH38 ?
20 months ago by geocarvalho ▴ 330
0
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1
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77k
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Comment: Comment: Extract Sub-Set Of Regions From Vcf File
24 months ago by geocarvalho ▴ 330
0
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0
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460
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Comment: C: Variant not annotated by ANNOVAR in the main transcript
2.4 years ago by geocarvalho ▴ 330
0
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1
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460
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Variant not annotated by ANNOVAR in the main transcript
Annovar Variant Annotation Transcript Exome
2.4 years ago by geocarvalho ▴ 330
1
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0
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19k
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Answer: A: Where to download blacklisted regions?
2.9 years ago by geocarvalho ▴ 330
0
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1
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1.1k
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Comment: C: Differential DNA methylation for each sample using Illumina HumanMethylation450
3.0 years ago by geocarvalho ▴ 330
6
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8
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1.1k
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Differential DNA methylation for each sample using Illumina HumanMethylation450 BeadChip dataset
R methylation humanmethylation450 limma
updated 3.0 years ago by 8.2k • written 3.0 years ago by ▴ 330
0
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1
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1.1k
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Comment: C: Differential DNA methylation for each sample using Illumina HumanMethylation450
3.0 years ago by geocarvalho ▴ 330
0
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0
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4.6k
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Comment: C: Using limma to find differentially methylated probes across clusters
3.0 years ago by geocarvalho ▴ 330
1
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1.6k
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Answer: A: CNV and pseudogenes
3.1 years ago by geocarvalho ▴ 330
0
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0
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196k
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Comment: C: How To Update R In Ubuntu ?
3.2 years ago by geocarvalho ▴ 330
9
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1
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77k
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Answer: A: Extract Sub-Set Of Regions From Vcf File
updated 3.4 years ago by 39k • written 5.7 years ago by ▴ 330
0
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0
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2.0k
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Answer: A: Trying to Identify larger indels from NGS data, FASTQ format
4.1 years ago by geocarvalho ▴ 330
1
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2.0k
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Comment: C: Identifying CNVs from targeted amplicon sequencing
4.2 years ago by geocarvalho ▴ 330
0
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1
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2.0k
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Comment: C: Identifying CNVs from targeted amplicon sequencing
4.2 years ago by geocarvalho ▴ 330
0
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0
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16k
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Comment: C: bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing m
4.3 years ago by geocarvalho ▴ 330
0
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1
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16k
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Comment: C: bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing m
4.3 years ago by geocarvalho ▴ 330
1
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2
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16k
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Comment: C: bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing m
4.3 years ago by geocarvalho ▴ 330
0
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0
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1.3k
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Answer: A: Annotation tool for cnvKit
4.5 years ago by geocarvalho ▴ 330
0
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0
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2.4k
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Comment: C: how to fix error in getGEO function?
4.8 years ago by geocarvalho ▴ 330
0
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1
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2.4k
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Comment: C: how to fix error in getGEO function?
updated 4.8 years ago by 34k • written 4.8 years ago by ▴ 330
0
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0
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1.4k
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Answer: A: Bioinformatics workshop or training courses
4.8 years ago by geocarvalho ▴ 330
0
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0
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1.2k
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Answer: A: Large deletions in exome sequencing data
5.0 years ago by geocarvalho ▴ 330
2
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1
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2.0k
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Answer: A: Identifying CNVs from targeted amplicon sequencing
5.0 years ago by geocarvalho ▴ 330
0
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0
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2.6k
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Answer: A: Plotting common SNPs from four individual from a vcf file
5.3 years ago by geocarvalho ▴ 330
2
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0
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2.2k
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Answer: A: R books with Quantitative Genetics examples?
5.3 years ago by geocarvalho ▴ 330
1
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0
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1.2k
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Answer: A: Packages/modules for CNV, Indels, SNPs analysis
5.3 years ago by geocarvalho ▴ 330
0
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0
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3.4k
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Comment: C: vcfeval Error: No sample name provided but calls is a multi-sample VCF
5.4 years ago by geocarvalho ▴ 330
4
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0
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11k
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Answer: A: List all available databases for ANNOVAR
5.4 years ago by geocarvalho ▴ 330
2
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0
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3.4k
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Answer: A: vcfeval Error: No sample name provided but calls is a multi-sample VCF
5.4 years ago by geocarvalho ▴ 330
0
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1
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1.6k
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Answer: A: How to start analyzing next-generation DNA and RNA sequencing data?
5.6 years ago by geocarvalho ▴ 330
1
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0
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1.4k
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Answer: A: Where can I find a sample analysis pipeline for DNA?
6.1 years ago by geocarvalho ▴ 330
1
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0
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1.9k
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Comment: C: Bioinformatics Data Analyst, University of Pennsylvania, Philadelphia
6.1 years ago by geocarvalho ▴ 330
0
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1
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1.4k
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Answer: A: Different reference and variant allele in IonTorrent variantCaller
6.1 years ago by geocarvalho ▴ 330
1
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0
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4.2k
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Answer: A: Copy Number Variation Tools
6.2 years ago by geocarvalho ▴ 330
0
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0
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5.9k
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Answer: A: Annotation of Structural Variants and CNVs
6.2 years ago by geocarvalho ▴ 330
46 results • Page 1 of 1
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