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Comment: C: STAR - genome indexes generation, genome file not created
7.9 years ago by Amitm ★ 2.3k
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9.0k
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Comment: C: STAR - genome indexes generation, genome file not created
7.9 years ago by Amitm ★ 2.3k
2
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2
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2.1k
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Comment: C: For RNA seq data analysis
7.9 years ago by Amitm ★ 2.3k
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0
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5.2k
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Comment: C: Somatic mutations from RNA-Seq data of tumor vs. normal
7.9 years ago by Amitm ★ 2.3k
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1
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2.4k
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Comment: C: viewing microRNA in IGV
8.0 years ago by Amitm ★ 2.3k
1
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1
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5.0k
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Comment: C: Clarification of good pipeline for transcriptome assembly of RNA-seq data
8.0 years ago by Amitm ★ 2.3k
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2
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5.0k
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Comment: C: Clarification of good pipeline for transcriptome assembly of RNA-seq data
8.0 years ago by Amitm ★ 2.3k
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0
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2.0k
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Comment: C: Will you critique/rate my mRNA seq alignment analysis?
8.0 years ago by Amitm ★ 2.3k
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0
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2.6k
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Comment: C: Annotate VCF with RepeatMasker
8.0 years ago by Amitm ★ 2.3k
2
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0
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4.0k
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Comment: C: I am trying to load a BAM file (Whole Genome) to IGV but I can't see anything
8.1 years ago by Amitm ★ 2.3k
1
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1
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5.4k
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Comment: C: Visualize Gene Fusions
8.1 years ago by Amitm ★ 2.3k
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0
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2.0k
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Comment: C: Un pack cel files
8.1 years ago by Amitm ★ 2.3k
0
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1
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8.2k
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Comment: C: RNA-seq RPKM significance cut off
8.1 years ago by Amitm ★ 2.3k
0
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1
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1.5k
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Comment: C: RNAseq assembly for diploid genome.
8.1 years ago by Amitm ★ 2.3k
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1
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2.7k
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Comment: C: Biology side of bioinformatics
8.1 years ago by Amitm ★ 2.3k
2
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1
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2.3k
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Comment: C: Cancer RNA-seq data
8.2 years ago by Amitm ★ 2.3k
1
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0
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5.3k
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Comment: C: How can I detect lncRNA?
8.2 years ago by Amitm ★ 2.3k
1
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0
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6.0k
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Comment: C: dbsnp in vcf format compatible with hg38
8.2 years ago by Amitm ★ 2.3k
2
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1
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6.3k
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Comment: C: Which source of annotation files to use, Ensemble or UCSC?
8.2 years ago by Amitm ★ 2.3k
1
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2
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5.3k
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Comment: C: How can I detect lncRNA?
8.2 years ago by Amitm ★ 2.3k
1
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2
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5.3k
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Comment: C: How can I detect lncRNA?
8.2 years ago by Amitm ★ 2.3k
0
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1
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5.3k
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Comment: C: How can I detect lncRNA?
8.2 years ago by Amitm ★ 2.3k
0
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1
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5.3k
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Comment: C: How can I detect lncRNA?
8.2 years ago by Amitm ★ 2.3k
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0
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2.8k
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Comment: C: MuTect --- with more stringent parameter settings I got more mutations -- Is thi
8.2 years ago by Amitm ★ 2.3k
4
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2
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8.9k
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Comment: C: From TCGA to GDC (Genomic data commons)
8.2 years ago by Amitm ★ 2.3k
1
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1
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2.0k
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Comment: C: TCGA exons data-de novo isoform assembly
8.2 years ago by Amitm ★ 2.3k
0
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0
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3.5k
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Comment: C: Clear explanation of parameter minReads2 in VarScan
8.2 years ago by Amitm ★ 2.3k
1
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1
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3.5k
views
Comment: C: Clear explanation of parameter minReads2 in VarScan
8.2 years ago by Amitm ★ 2.3k
1
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1
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3.5k
views
Comment: C: Clear explanation of parameter minReads2 in VarScan
8.2 years ago by Amitm ★ 2.3k
0
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1
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3.5k
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Comment: C: Clear explanation of parameter minReads2 in VarScan
8.2 years ago by Amitm ★ 2.3k
1
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1
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2.0k
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Comment: C: TCGA exons data-de novo isoform assembly
8.2 years ago by Amitm ★ 2.3k
1
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1
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1.9k
views
Comment: C: getting reads counts at RefSeq genes
8.3 years ago by Amitm ★ 2.3k
1
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1
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2.0k
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Comment: C: removing dbsnp for indel vcf
8.3 years ago by Amitm ★ 2.3k
0
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0
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3.6k
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Comment: C: Does CDS, start_codon and stop_codon in gtf affect transcriptome assembly by Str
8.4 years ago by Amitm ★ 2.3k
0
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1
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3.6k
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Comment: C: Does CDS, start_codon and stop_codon in gtf affect transcriptome assembly by Str
8.4 years ago by Amitm ★ 2.3k
0
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0
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2.3k
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Comment: C: Few genes with many reads aligned,
8.4 years ago by Amitm ★ 2.3k
1
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0
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2.3k
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Comment: C: Few genes with many reads aligned,
8.4 years ago by Amitm ★ 2.3k
1
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0
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7.3k
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Comment: C: Picard Markduplicates output
8.4 years ago by Amitm ★ 2.3k
0
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1
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3.5k
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Comment: C: Non-cancer somatic mutation calling
8.4 years ago by Amitm ★ 2.3k
0
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1
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3.6k
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Comment: C: ADTEx coverage issue
8.4 years ago by Amitm ★ 2.3k
0
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1
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3.6k
views
Comment: C: ADTEx coverage issue
8.4 years ago by Amitm ★ 2.3k
0
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0
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2.8k
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Comment: C: non human contaminants in sequencing
8.4 years ago by Amitm ★ 2.3k
0
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1
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3.6k
views
Comment: C: ADTEx coverage issue
8.4 years ago by Amitm ★ 2.3k
0
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1
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2.9k
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Comment: C: High percentage of UTR mutations in RNAseq
8.5 years ago by Amitm ★ 2.3k
0
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1
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3.2k
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Comment: C: BLAT: how to select best hit at one genomic position? (queries are repeats)
8.5 years ago by Amitm ★ 2.3k
1
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1
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7.1k
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Comment: C: New to BEDtools, can't get intersect to work
8.5 years ago by Amitm ★ 2.3k
0
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1
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2.9k
views
Comment: C: High percentage of UTR mutations in RNAseq
8.5 years ago by Amitm ★ 2.3k
1
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0
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2.5k
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Comment: C: How to start Gene Analysis?
8.5 years ago by Amitm ★ 2.3k
0
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0
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1.2k
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Comment: C: Proteins types used in ENCODE
8.5 years ago by Amitm ★ 2.3k
0
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0
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2.4k
views
Comment: C: Infer loss of heterozygosity from SNP variant frequencies
8.5 years ago by Amitm ★ 2.3k
197 results • Page 3 of 4
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