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Answer: Answer: Assembly of oxford nanopore sequencing data
2.3 years ago by H.Hasani ▴ 990
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Answer: A: How I produce such a plot in R
3.7 years ago by H.Hasani ▴ 990
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3.6k
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Answer: A: Statistical test for overlap
3.9 years ago by H.Hasani ▴ 990
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963
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Answer: C: Survival analysis, K-M vs actuarial
3.9 years ago by H.Hasani ▴ 990
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Answer: C: R: pedigree analysis
4.2 years ago by H.Hasani ▴ 990
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1.0k
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Answer: A: Create a heatmap
4.2 years ago by H.Hasani ▴ 990
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Answer: A: How extract gene TPM from GTEx?
4.3 years ago by H.Hasani ▴ 990
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7.0k
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Answer: A: SNPs located in promoter region. OR exon, intron, 5'UTR, 3'UTR
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 990
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Answer: A: How many SNPs are sufficiant for covering?
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 990
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4.2k
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Answer: A: No significantly mutated genes in Mutsig
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 990
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699
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Answer: A: ucsc genome browser variants read
4.6 years ago by H.Hasani ▴ 990
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1.4k
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Answer: A: How to calculate allele counts(Ref and alt) using a target bed file and aligned
4.8 years ago by H.Hasani ▴ 990
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1.3k
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Answer: A: Barplot with base point as 0.5
4.9 years ago by H.Hasani ▴ 990
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944
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Answer: A: Mutated gene based pathway enrichment
4.9 years ago by H.Hasani ▴ 990
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1.8k
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Answer: A: Getting this specific information from gene- annotation enrichment analysis
4.9 years ago by H.Hasani ▴ 990
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2.3k
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Answer: A: venndiagram `Error in draw.quintuple.venn`?
5.1 years ago by H.Hasani ▴ 990
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2.9k
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Answer: A: Lolliplot graph for mutations
5.4 years ago by H.Hasani ▴ 990
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7.7k
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Answer: A: download tumor and normal data from TCGA
5.4 years ago by H.Hasani ▴ 990
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1
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2.5k
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Answer: A: Bioinformatics terms that might be confusing for beginners
5.6 years ago by H.Hasani ▴ 990
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2.0k
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Answer: A: Detection of SNPs
6.0 years ago by H.Hasani ▴ 990
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33k
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Answer: A: In simple words - what is k-mer??
6.4 years ago by H.Hasani ▴ 990
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1.5k
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Answer: A: functional variant discovery after GATK variant calling
6.9 years ago by H.Hasani ▴ 990
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1.7k
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Answer: A: Broad rules of thumb on # of variations
6.9 years ago by H.Hasani ▴ 990
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6.2k
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Answer: A: samtools view region
6.9 years ago by H.Hasani ▴ 990
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2.5k
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Answer: A: TCGA raw counts DexSeq
6.9 years ago by H.Hasani ▴ 990
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2.2k
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Answer: A: how to replace certain column name based on another file
7.6 years ago by H.Hasani ▴ 990
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4.4k
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Answer: A: csv into genome browser
7.6 years ago by H.Hasani ▴ 990
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12k
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Answer: A: How to avoid conversion of gene symbols to date format in Excel
7.6 years ago by H.Hasani ▴ 990
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1.6k
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Answer: A: Plot chromossomes in R
7.6 years ago by H.Hasani ▴ 990
3
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2
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21k
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Answer: A: What Is Your Favorite Question To Ask When Interviewing Potential Bioinformatici
7.8 years ago by H.Hasani ▴ 990
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2.8k
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Answer: A: MuTect is giving strikingly different results
7.8 years ago by H.Hasani ▴ 990
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7.8k
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Answer: A: Allele Specific Events
7.9 years ago by H.Hasani ▴ 990
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Answer: A: Why are SNPs with small effect sizes a problem for GWAS?
7.9 years ago by H.Hasani ▴ 990
3
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6.0k
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Answer: A: Beginner in Bioinformatics / computational biology field
7.9 years ago by H.Hasani ▴ 990
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9.1k
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Answer: A: Finding overlapping ranges in R
7.9 years ago by H.Hasani ▴ 990
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0
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12k
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Answer: Answer: Map genetic mutations to protein domain/structure
updated 2.1 years ago by 43k • written 8.0 years ago by ▴ 990
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2.6k
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Answer: A: Presenting "Role of genomics in cancer" to graduate students from different fiel
8.1 years ago by H.Hasani ▴ 990
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1
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1.9k
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Answer: A: ncRNAs with CDS in NCBI
8.1 years ago by H.Hasani ▴ 990
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1
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2.3k
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Answer: A: How to convert gene names into ID symbol in NCBI
8.1 years ago by H.Hasani ▴ 990
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1.7k
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Answer: A: Genomic variation course at the EBI
8.1 years ago by H.Hasani ▴ 990
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1
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4.3k
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Answer: A: Is reference genome same for DNA and RNA sequence alignment
8.1 years ago by H.Hasani ▴ 990
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1
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2.8k
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Answer: A: Are there recommended steps if MuSiC reports too many significantly mutated gene
8.1 years ago by H.Hasani ▴ 990
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2.5k
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Answer: A: I'm in a Masters of Bioinformatics Program and wanted to ask everyone for advice
8.1 years ago by H.Hasani ▴ 990
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0
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2.3k
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Answer: A: Sanger sequencing results don't match the reference and alt alleles?
8.1 years ago by H.Hasani ▴ 990
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1
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4.6k
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Answer: A: Do I need to use hg19 or hg38 reference for performing variant calling analysis
8.2 years ago by H.Hasani ▴ 990
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1
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3.5k
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Answer: A: How to find exact allele frequency for the SNP/indel variants ?
8.2 years ago by H.Hasani ▴ 990
2
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7.7k
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Answer: A: Difference Between GATK, Freebayes and SAMtools mpileup
8.2 years ago by H.Hasani ▴ 990
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2.8k
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Answer: A: Allele frequencies in pedigrees
8.4 years ago by H.Hasani ▴ 990
2
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0
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2.9k
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Answer: A: SNP zygosity from RNA-Seq data (BAM file)
8.4 years ago by H.Hasani ▴ 990
49 results • Page 1 of 1
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