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Comment: C: hisat2 and htseq-count
8.5 years ago by WouterDeCoster 48k
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1.8k
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Comment: C: gene family evolution
8.5 years ago by WouterDeCoster 48k
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1.9k
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Comment: C: vcf at variable sites only
8.5 years ago by WouterDeCoster 48k
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5.3k
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Comment: C: genomics overlap python error
8.5 years ago by WouterDeCoster 48k
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5.3k
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Comment: C: genomics overlap python error
8.5 years ago by WouterDeCoster 48k
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5.3k
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Comment: C: genomics overlap python error
8.5 years ago by WouterDeCoster 48k
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5.0k
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Comment: C: Deseq2 differential result
8.5 years ago by WouterDeCoster 48k
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1
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5.3k
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Comment: C: genomics overlap python error
8.5 years ago by WouterDeCoster 48k
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2.0k
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Comment: C: How could make this super cool p-value for all genes for specific query by R or
8.5 years ago by WouterDeCoster 48k
1
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1
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5.3k
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Comment: C: genomics overlap python error
8.5 years ago by WouterDeCoster 48k
3
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1
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11k
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Answer: A: Best way to merge RNA-seq data from two sequencing runs of the same samples
8.5 years ago by WouterDeCoster 48k
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5.0k
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Comment: C: Deseq2 differential result
8.5 years ago by WouterDeCoster 48k
0
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1.6k
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Comment: C: Per base statistics on an RNAseq bam file
8.5 years ago by WouterDeCoster 48k
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1.5k
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Comment: C: Icoshift is not working in Pathomx
8.5 years ago by WouterDeCoster 48k
0
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1
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5.8k
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Comment: C: Rearranging order of descriptors in fasta file header
8.5 years ago by WouterDeCoster 48k
0
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0
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21k
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Comment: C: NGS files' shrinkage software: ALAPY Compressor, only fastq files so far =)
8.5 years ago by WouterDeCoster 48k
1
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1
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21k
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Comment: C: NGS files' shrinkage software: ALAPY Compressor, only fastq files so far =)
8.5 years ago by WouterDeCoster 48k
0
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2.6k
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Comment: C: how to find ratio of cases vs control per variant from a vcf file
8.5 years ago by WouterDeCoster 48k
1
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1
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4.6k
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Comment: C: EOF marker is absent
8.5 years ago by WouterDeCoster 48k
2
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0
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2.6k
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Comment: C: how to find ratio of cases vs control per variant from a vcf file
8.5 years ago by WouterDeCoster 48k
0
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0
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3.1k
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Comment: C: Identify recessive conditions from VCF files
8.5 years ago by WouterDeCoster 48k
1
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1
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1.7k
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Comment: C: SNP data analysis
8.5 years ago by WouterDeCoster 48k
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1.3k
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Answer: A: Pool male and female individuals for de novo transcriptome assembly?
8.5 years ago by WouterDeCoster 48k
3
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2.7k
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Answer: A: Genes responsible for cancers
8.5 years ago by WouterDeCoster 48k
1
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1
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5.8k
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Answer: A: Rearranging order of descriptors in fasta file header
8.6 years ago by WouterDeCoster 48k
0
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1
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5.8k
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Comment: C: Rearranging order of descriptors in fasta file header
8.6 years ago by WouterDeCoster 48k
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1
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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2
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5.8k
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Comment: C: Rearranging order of descriptors in fasta file header
8.6 years ago by WouterDeCoster 48k
0
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1
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4.3k
views
Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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1
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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0
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
2
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0
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2.1k
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Comment: C: How to learn Basic languge for operating DNA/RNA seq analysis tools?
8.6 years ago by WouterDeCoster 48k
0
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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0
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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0
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4.5k
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Comment: C: Upgrade Ubuntu 16.04 to Bio Linux 8
8.6 years ago by WouterDeCoster 48k
0
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1
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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3
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
1
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0
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2.7k
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Comment: C: No positive results after SAM
8.6 years ago by WouterDeCoster 48k
1
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2
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4.3k
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Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
3
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0
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2.1k
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Answer: A: How to learn Basic languge for operating DNA/RNA seq analysis tools?
8.6 years ago by WouterDeCoster 48k
2
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1
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2.1k
views
Comment: C: How to learn Basic languge for operating DNA/RNA seq analysis tools?
8.6 years ago by WouterDeCoster 48k
0
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2
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3.3k
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Comment: C: How to splice introne sequences for each transcript.
8.6 years ago by WouterDeCoster 48k
0
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0
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2.8k
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Comment: C: Merge two BAM files with different but overlapping reference sequences?
8.6 years ago by WouterDeCoster 48k
3
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1
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6.7k
views
Answer: A: How to map the reads from a Bam file to another reference genome????
8.6 years ago by WouterDeCoster 48k
1
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0
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3.0k
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Comment: C: Differentially Expressed Genes Analysis with RNA-Seq data
8.6 years ago by WouterDeCoster 48k
0
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0
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4.1k
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Comment: C: How to add a legend to the heatmap?
8.6 years ago by WouterDeCoster 48k
0
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2
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3.3k
views
Comment: C: How to splice introne sequences for each transcript.
8.6 years ago by WouterDeCoster 48k
0
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1
reply
3.3k
views
Comment: A: How to splice introne sequences for each transcript.
8.6 years ago by WouterDeCoster 48k
0
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1
reply
4.3k
views
Comment: C: Is my file created completely
8.6 years ago by WouterDeCoster 48k
0
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0
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21k
views
Comment: C: NGS files' shrinkage software: ALAPY Compressor, only fastq files so far =)
8.6 years ago by WouterDeCoster 48k
7,263 results • Page 83 of 146
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