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Comment: Comment: how to count variants par sample per chromosome in a vcf file?
3.7 years ago by Leandro Lima ▴ 970
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1
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26k
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Comment: C: intersect VCF files
4.9 years ago by Leandro Lima ▴ 970
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2.7k
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Comment: C: Alternatives to Broad's DAPPLE tool?
updated 5.0 years ago by 44k • written 8.9 years ago by ▴ 970
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2.1k
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Comment: C: XHMM on whole genome sequencing data
updated 6.2 years ago by 44k • written 8.8 years ago by ▴ 970
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39k
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Comment: C: List Of Genome Sequencing Centers/Institutes
6.6 years ago by Leandro Lima ▴ 970
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8.3k
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Comment: C: How to use GRCh38 as reference for Annotating the variants using Annovar?
6.6 years ago by Leandro Lima ▴ 970
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1.4k
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Comment: C: Machine Learning/Deep Learning approaches to integrate genotype and annotation i
6.9 years ago by Leandro Lima ▴ 970
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10k
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Comment: C: ./ Vs "0/0" In Vcf Files
7.0 years ago by Leandro Lima ▴ 970
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5.0k
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Comment: Comment: CNV frequencies and MAF
updated 2.8 years ago by 44k • written 7.8 years ago by ▴ 970
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1
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2.9k
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Comment: C: Semantic Similarity against all MeSH categories
7.8 years ago by Leandro Lima ▴ 970
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1
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2.9k
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Comment: C: Semantic Similarity against all MeSH categories
8.0 years ago by Leandro Lima ▴ 970
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17k
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Comment: C: Gatk - Haplotypecaller Is So Slow, What Is Faster And As Good?
8.1 years ago by Leandro Lima ▴ 970
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2.1k
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Comment: C: help geometadb r package
8.1 years ago by Leandro Lima ▴ 970
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5.0k
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Comment: C: How to search/filter GEO datasets according platform (Illumina/Affymetrix)
8.2 years ago by Leandro Lima ▴ 970
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7.5k
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Comment: C: Tools for SV & CNV detection
8.4 years ago by Leandro Lima ▴ 970
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1
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2.6k
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Comment: C: Existing methods to evaluate the performance of SV/CNV calling tools
8.6 years ago by Leandro Lima ▴ 970
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7.5k
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Comment: C: Tools for SV & CNV detection
8.8 years ago by Leandro Lima ▴ 970
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6.2k
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Comment: C: CNVnator installation error
8.9 years ago by Leandro Lima ▴ 970
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2.1k
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Comment: C: Pack your bags and move to Portland!! Multiple network biology/pathway informati
9.0 years ago by Leandro Lima ▴ 970
6
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3
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42k
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Comment: C: Difference Between "Mate Pair" And "Pair-End"
9.0 years ago by Leandro Lima ▴ 970
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4.9k
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Comment: C: samtools error file
9.1 years ago by Leandro Lima ▴ 970
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2.6k
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Comment: C: Simulating Cnv Into Genome Reference
9.3 years ago by Leandro Lima ▴ 970
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2.8k
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Comment: Comment: Cnv Data Set
updated 2.2 years ago by 44k • written 9.3 years ago by ▴ 970
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5.6k
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Comment: C: Short Read Simulator For Cnv Indel?
9.3 years ago by Leandro Lima ▴ 970
2
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1
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13k
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Comment: Comment: bedtools 2.0 merge - "unable to open file or unable to determine types"
updated 2.9 years ago by 44k • written 9.7 years ago by ▴ 970
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7.6k
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Comment: C: How To Reorder Bam File Contigs For The Gatk Pipeline
10.2 years ago by Leandro Lima ▴ 970
2
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1
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20k
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Comment: C: Multi-Panel Heatmaps In R
11.1 years ago by Leandro Lima ▴ 970
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1
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3.8k
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Comment: C: How To Visualize The Quality Of Sequencing Data In Colorspace (Solid) Format?
11.2 years ago by Leandro Lima ▴ 970
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3.4k
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Comment: C: Gwas3D: Detecting Human Regulatory Variants By Combining Chromosome Conformation
11.4 years ago by Leandro Lima ▴ 970
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4.8k
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Comment: C: Biology Introduction For A Computer Scientist
11.5 years ago by Leandro Lima ▴ 970
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2.1k
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Comment: C: Selecting Gene Subsets Such That No Two Genes Occur In The Same Set More Than "T
11.6 years ago by Leandro Lima ▴ 970
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2.1k
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Comment: C: Selecting Gene Subsets Such That No Two Genes Occur In The Same Set More Than "T
11.6 years ago by Leandro Lima ▴ 970
1
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0
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5.8k
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Comment: C: Difficult To Download Gene Sequences From Ncbi
11.6 years ago by Leandro Lima ▴ 970
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1
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3.1k
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Comment: C: How To Make Cytoscape Export Network In Cluster Format (Non-Sif)
11.6 years ago by Leandro Lima ▴ 970
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1
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3.1k
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Comment: C: How To Make Cytoscape Export Network In Cluster Format (Non-Sif)
11.6 years ago by Leandro Lima ▴ 970
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11k
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Comment: C: Identifying Viral Sequences In Next Generation Sequencing Data
11.6 years ago by Leandro Lima ▴ 970
0
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1
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11k
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Comment: C: Identifying Viral Sequences In Next Generation Sequencing Data
11.6 years ago by Leandro Lima ▴ 970
0
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0
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5.1k
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Comment: C: How To Align Then Visualize The Alignment Of Rna Sequences With R Or Python
11.7 years ago by Leandro Lima ▴ 970
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1
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3.8k
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Comment: C: [Ncbi Entrez] Retrieving Complete Genome Informations From Ncbi Genome
11.7 years ago by Leandro Lima ▴ 970
1
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0
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14k
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Comment: C: Get Go Terms From Python
11.8 years ago by Leandro Lima ▴ 970
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0
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20k
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Comment: C: How To Fetch Genomics Sequence Using Coordinates In Biopython
11.8 years ago by Leandro Lima ▴ 970
2
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3.4k
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Comment: C: Other Examples Of Successful Bioinformatics-Focused "Professional" Networks?
11.9 years ago by Leandro Lima ▴ 970
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4.7k
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Comment: C: Error With Kegg Api Sample Code For Python
11.9 years ago by Leandro Lima ▴ 970
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5.2k
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Comment: C: Find Enriched Function In Go Terms
12.0 years ago by Leandro Lima ▴ 970
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0
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7.8k
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Comment: C: Generating A Gene Ontology Network For Cytoscape
12.0 years ago by Leandro Lima ▴ 970
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