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Comment: C: Perl basic script and project
9.1 years ago by GouthamAtla 12k
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2.6k
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Answer: A: How to calculate reference allele frequency in pyvcf and print for all line?
9.1 years ago by GouthamAtla 12k
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7.6k
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Comment: C: Time Course RNA-Seq
9.1 years ago by GouthamAtla 12k
1
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0
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2.3k
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Comment: C: Looking for Population Genetics Simulation Software
9.1 years ago by GouthamAtla 12k
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4.3k
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Answer: A: Counts from cuffdiff VS featurecounts
9.1 years ago by GouthamAtla 12k
3
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5.1k
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Answer: A: Calculating number of reads in a specific region from sam file
9.2 years ago by GouthamAtla 12k
0
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4.8k
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Comment: C: I am trying to load a BAM file (Whole Genome) to IGV but I can't see anything
9.2 years ago by GouthamAtla 12k
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1
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2.0k
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Comment: C: Length of reads in a RNAseq experiment
9.2 years ago by GouthamAtla 12k
2
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0
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2.3k
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Comment: C: Differentiall analysis of chip-deq data
9.2 years ago by GouthamAtla 12k
0
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0
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9.6k
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Comment: C: ENCODE ATAC-seq pipeline peak calling
9.2 years ago by GouthamAtla 12k
0
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1
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2.5k
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Comment: C: why we performed cufflinks and what does the assembled transcripts mean?
9.2 years ago by GouthamAtla 12k
0
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1
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6.9k
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Comment: C: Can GATK read compressed vcf files?
9.2 years ago by GouthamAtla 12k
2
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0
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2.5k
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Answer: A: WGCNA on Small RNA-Seq data
9.2 years ago by GouthamAtla 12k
0
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0
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1.8k
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Comment: C: I have start and end position of sequences, want to remove redundancy
9.2 years ago by GouthamAtla 12k
0
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0
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7.2k
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Comment: C: How to merge two vcf files, which have same variants but don't regard same varia
9.2 years ago by GouthamAtla 12k
2
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1
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7.2k
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Comment: C: How to merge two vcf files, which have same variants but don't regard same varia
9.2 years ago by GouthamAtla 12k
4
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2
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1.8k
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Answer: A: I have start and end position of sequences, want to remove redundancy
9.2 years ago by GouthamAtla 12k
0
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0
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4.0k
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Comment: C: why the featurecounts result is empty
9.2 years ago by GouthamAtla 12k
0
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0
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2.1k
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Comment: C: what is the mean count number in IGV RefSeq Genes track
9.2 years ago by GouthamAtla 12k
0
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3
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4.0k
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Comment: C: why the featurecounts result is empty
9.2 years ago by GouthamAtla 12k
1
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0
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2.4k
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Comment: C: using python script to analyze ht-seq data
9.2 years ago by GouthamAtla 12k
1
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1
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9.6k
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Comment: C: ENCODE ATAC-seq pipeline peak calling
9.2 years ago by GouthamAtla 12k
0
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1
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9.6k
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Comment: C: ENCODE ATAC-seq pipeline peak calling
9.2 years ago by GouthamAtla 12k
0
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0
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6.9k
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Comment: C: Detecting bacterial TSS from RNA-Seq data, how?
9.2 years ago by GouthamAtla 12k
0
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2
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6.9k
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Answer: A: Detecting bacterial TSS from RNA-Seq data, how?
9.2 years ago by GouthamAtla 12k
0
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1
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6.9k
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Comment: C: Detecting bacterial TSS from RNA-Seq data, how?
9.2 years ago by GouthamAtla 12k
1
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1
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2.6k
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Comment: C: feeding RPKM values into DE analysis tools
9.2 years ago by GouthamAtla 12k
26
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8
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7.1k
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7 follow
How Complex It Is To Analyze Ngs Data ?
ngs
updated 2.7 years ago by 45k • written 12.2 years ago by 12k
3
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1
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7.1k
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Comment: C: How Complex It Is To Analyze Ngs Data ?
9.2 years ago by GouthamAtla 12k
3
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1
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13k
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Answer: C: How to add custom fields to the VCF files?
9.2 years ago by GouthamAtla 12k
1
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1
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2.7k
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Comment: C: number of Unique reads in bowtie2 alignment
9.2 years ago by GouthamAtla 12k
0
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2
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8.4k
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Answer: C: Step by step instructions to phase with Eagle?
9.2 years ago by GouthamAtla 12k
0
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0
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13k
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Comment: C: How to add custom fields to the VCF files?
9.2 years ago by GouthamAtla 12k
0
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0
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2.2k
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Comment: C: GWAS: how to do hypothesis testing is phenotypes are continuous?
9.2 years ago by GouthamAtla 12k
1
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1
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5.1k
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Comment: C: VCF simplify INFO
9.2 years ago by GouthamAtla 12k
0
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1
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5.1k
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Comment: C: VCF simplify INFO
9.2 years ago by GouthamAtla 12k
0
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1
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2.2k
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Comment: C: Is there a way to extract sites that are perfectly aligned to the reference geno
9.2 years ago by GouthamAtla 12k
1
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2
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7.7k
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Comment: C: I got low overall alignment rate running HiSAT2
9.2 years ago by GouthamAtla 12k
0
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0
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3.3k
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Answer: C: unmapped reads from Tophat
9.2 years ago by GouthamAtla 12k
1
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1
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5.1k
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Comment: C: VCF simplify INFO
9.2 years ago by GouthamAtla 12k
0
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1
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5.1k
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Comment: C: VCF simplify INFO
9.2 years ago by GouthamAtla 12k
1
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0
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7.5k
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Comment: C: PCA plot- R/Bioconductor-Deseq2
9.2 years ago by GouthamAtla 12k
0
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0
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3.4k
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Comment: C: Heatmap from chromosome co-ordinates
9.2 years ago by GouthamAtla 12k
0
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1
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3.8k
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Comment: C: finding significance between transcripts in a RNA-Seq experiment
9.2 years ago by GouthamAtla 12k
0
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0
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3.1k
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Comment: C: repeated read ids from Illumina MiniSeq fastq.gz files?
9.2 years ago by GouthamAtla 12k
1
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0
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1.5k
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Comment: C: Cancer Epigenetics and related articles
9.2 years ago by GouthamAtla 12k
0
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1
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3.1k
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Comment: C: repeated read ids from Illumina MiniSeq fastq.gz files?
9.2 years ago by GouthamAtla 12k
0
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1
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2.1k
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Comment: C: Truncate RNASeq data to get similar abundance
9.2 years ago by GouthamAtla 12k
2
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1
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18k
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Comment: C: convert text file to fasta file
9.2 years ago by GouthamAtla 12k
2
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1
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2.1k
views
Comment: C: Truncate RNASeq data to get similar abundance
9.2 years ago by GouthamAtla 12k
1,492 results • Page 13 of 30
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