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Comment: C: TCGA raw counts DexSeq
6.9 years ago by H.Hasani ▴ 990
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1
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6.2k
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Comment: C: samtools view region
6.9 years ago by H.Hasani ▴ 990
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9.9k
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Comment: C: GEO datasets: Raw data is available on Series record
6.9 years ago by H.Hasani ▴ 990
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1
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9.9k
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Comment: C: GEO datasets: Raw data is available on Series record
6.9 years ago by H.Hasani ▴ 990
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2
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3.5k
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Comment: C: Interpreting unusual-looking mean-variance plot from EdgeR
7.0 years ago by H.Hasani ▴ 990
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4.1k
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Comment: C: clusterProfiler (KEGG Enrichment Analysis) error
7.0 years ago by H.Hasani ▴ 990
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10k
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Comment: C: Bowtie2 error with single end mapping
7.1 years ago by H.Hasani ▴ 990
3
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1
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1.6k
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Comment: C: How to predict mutation without using variant callers like GATK, Mutect?
7.2 years ago by H.Hasani ▴ 990
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1.1k
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Comment: C: variant filtration criteria
7.2 years ago by H.Hasani ▴ 990
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1
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27k
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Comment: C: Duplicated Reads In Rna-Seq Experiment
7.2 years ago by H.Hasani ▴ 990
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1.7k
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Comment: C: SNP Data Quality control
7.2 years ago by H.Hasani ▴ 990
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4.8k
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Comment: C: Chip-Seq Enrichment Profile Significance?
7.2 years ago by H.Hasani ▴ 990
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1
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1.6k
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Comment: C: chi squared test for comparing two groups of proteins
7.5 years ago by H.Hasani ▴ 990
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3.5k
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Comment: C: Overrepresented sequence in RNA-seq only in R2
7.5 years ago by H.Hasani ▴ 990
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1
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3.1k
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Comment: C: Statistical test to compare expression change in a subgroup of genes versus all
7.6 years ago by H.Hasani ▴ 990
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1
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3.1k
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Comment: C: Statistical test to compare expression change in a subgroup of genes versus all
7.6 years ago by H.Hasani ▴ 990
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2.3k
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Comment: C: How to map by bwa with 50 mismatches?
7.6 years ago by H.Hasani ▴ 990
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4.4k
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Comment: C: csv into genome browser
7.6 years ago by H.Hasani ▴ 990
1
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1.7k
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Comment: C: cbioPortal MutationMapper protein domain annotation not up-to-date
7.6 years ago by H.Hasani ▴ 990
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1
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2.2k
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Comment: C: Looking for a cancer dataset for RNA-Seq workshop
7.6 years ago by H.Hasani ▴ 990
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1.6k
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Comment: C: fasta sequence position
7.6 years ago by H.Hasani ▴ 990
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1.4k
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Comment: C: Protein structure and snps
7.6 years ago by H.Hasani ▴ 990
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14k
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Comment: C: Search dbSNP for hg19 based coordinates
7.7 years ago by H.Hasani ▴ 990
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3.8k
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Comment: C: SNP genotyping and analysis of association with phenotype
7.7 years ago by H.Hasani ▴ 990
1
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7.9k
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Comment: C: Simulating Rna-Seq Reads
7.8 years ago by H.Hasani ▴ 990
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0
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8.4k
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Comment: C: How To Install BioPerl Without Root Privileges in Ubuntu/Linxu
7.8 years ago by H.Hasani ▴ 990
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1
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2.2k
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Comment: C: How do scientists identify new genes/SNP as candidates for GWAS studies?
7.9 years ago by H.Hasani ▴ 990
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1
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2.2k
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Comment: C: How do scientists identify new genes/SNP as candidates for GWAS studies?
7.9 years ago by H.Hasani ▴ 990
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0
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2.7k
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Comment: C: How many samples are there in 1000 genome project VCF file?
7.9 years ago by H.Hasani ▴ 990
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2.7k
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Comment: C: Visualizing mutations burden vs. gene expression
7.9 years ago by H.Hasani ▴ 990
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1
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2.7k
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Comment: C: Visualizing mutations burden vs. gene expression
7.9 years ago by H.Hasani ▴ 990
1
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2.7k
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Comment: C: Visualizing mutations burden vs. gene expression
7.9 years ago by H.Hasani ▴ 990
1
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0
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2.7k
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Comment: C: Visualizing mutations burden vs. gene expression
7.9 years ago by H.Hasani ▴ 990
0
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1
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7.4k
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Comment: C: R stat heatmap problem
7.9 years ago by H.Hasani ▴ 990
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1
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5.1k
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Comment: C: VCF file without SNPs
7.9 years ago by H.Hasani ▴ 990
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1
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5.1k
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Comment: C: VCF file without SNPs
7.9 years ago by H.Hasani ▴ 990
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5.1k
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Comment: C: VCF file without SNPs
7.9 years ago by H.Hasani ▴ 990
1
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1
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6.4k
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Comment: C: Does anyone use Python for variant calling?
7.9 years ago by H.Hasani ▴ 990
1
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5.1k
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Comment: C: VCF file without SNPs
7.9 years ago by H.Hasani ▴ 990
0
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0
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4.4k
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Comment: C: csv into genome browser
7.9 years ago by H.Hasani ▴ 990
0
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0
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4.4k
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Comment: C: csv into genome browser
7.9 years ago by H.Hasani ▴ 990
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1
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4.4k
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Comment: C: csv into genome browser
7.9 years ago by H.Hasani ▴ 990
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0
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1.5k
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Comment: C: Genes by Protein Domain
8.0 years ago by H.Hasani ▴ 990
2
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1.5k
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Comment: C: Genes by Protein Domain
8.0 years ago by H.Hasani ▴ 990
3
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0
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11k
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Comment: C: Determine sex from vcf file (or sequencing data)
8.0 years ago by H.Hasani ▴ 990
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3.0k
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Comment: C: How to Specify Genome Build in MutSigCV Input ?
8.0 years ago by H.Hasani ▴ 990
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2.2k
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Comment: C: ORF search gives negative start value
8.1 years ago by H.Hasani ▴ 990
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3.8k
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Comment: A: vcf files in gatk not showing data lines
8.1 years ago by H.Hasani ▴ 990
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1.7k
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Comment: C: Help with looking at mutations from RNA-SEQ data
8.1 years ago by H.Hasani ▴ 990
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0
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2.0k
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Comment: C: include indels along with SNPs in linear model
8.1 years ago by H.Hasani ▴ 990
126 results • Page 2 of 3
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