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Comment: C: Very low p-values
8.5 years ago by WouterDeCoster 48k
2
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5.6k
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Comment: C: Are these false somatic variants? Visual inspection with IGV
8.5 years ago by WouterDeCoster 48k
2
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2.8k
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Comment: C: Sequence alignment algorithm for big size genes in MATLAB
8.5 years ago by WouterDeCoster 48k
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3.1k
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Comment: C: How to find novel gene/isoform in 1 RNA-SEQ sample?
8.5 years ago by WouterDeCoster 48k
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2.7k
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Comment: C: to much time for using cufflinks
8.5 years ago by WouterDeCoster 48k
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7.0k
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Comment: C: Grep Position List
8.5 years ago by WouterDeCoster 48k
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7.7k
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Comment: C: Circos histogram from SNP.VCf file
8.5 years ago by WouterDeCoster 48k
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1.8k
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Comment: C: How to find and download the Database from a particular gene in NCBI
8.5 years ago by WouterDeCoster 48k
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1
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1.8k
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Comment: C: How to find and download the Database from a particular gene in NCBI
8.5 years ago by WouterDeCoster 48k
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4.9k
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Comment: C: Blast multiple sequences with Biopython qblast
8.5 years ago by WouterDeCoster 48k
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8.5k
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Comment: C: Is annotation of enhancers to nearest gene pointless?
8.5 years ago by WouterDeCoster 48k
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1
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2.2k
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Comment: C: Script to report GC content of the island returned by SICER
8.5 years ago by WouterDeCoster 48k
1
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1
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2.2k
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Answer: A: Script to report GC content of the island returned by SICER
8.5 years ago by WouterDeCoster 48k
4
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1
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8.5k
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Comment: C: Is annotation of enhancers to nearest gene pointless?
8.5 years ago by WouterDeCoster 48k
1
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1
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8.5k
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Comment: C: Is annotation of enhancers to nearest gene pointless?
8.5 years ago by WouterDeCoster 48k
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2.4k
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Comment: C: Question: combining RNAseq data from different platforms
8.5 years ago by WouterDeCoster 48k
1
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2.4k
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Comment: C: Splitting the Spliced reads from genome Alignment
8.5 years ago by WouterDeCoster 48k
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3.8k
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Comment: C: htseq read count zero ?
8.5 years ago by WouterDeCoster 48k
1
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1
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3.0k
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Comment: C: Does BioMart based go-terms contain any insignificant go-terms ?
8.5 years ago by WouterDeCoster 48k
0
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3.0k
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Comment: C: Does BioMart based go-terms contain any insignificant go-terms ?
8.5 years ago by WouterDeCoster 48k
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1.9k
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Comment: C: How to extract trinity gene id
8.5 years ago by WouterDeCoster 48k
3
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1
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1.9k
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Answer: C: How to extract trinity gene id
8.5 years ago by WouterDeCoster 48k
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1
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1.9k
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Comment: C: How to extract trinity gene id
8.5 years ago by WouterDeCoster 48k
0
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1
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1.9k
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Comment: C: How to extract trinity gene id
8.5 years ago by WouterDeCoster 48k
0
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1.6k
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Comment: C: How to delete an answer
8.5 years ago by WouterDeCoster 48k
1
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1
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1.6k
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Answer: A: How to delete an answer
8.5 years ago by WouterDeCoster 48k
1
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980
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Comment: C: Bioinformatics tools for genetic diversity
8.5 years ago by WouterDeCoster 48k
0
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1.7k
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Comment: C: Sequence extraction based on coordinates
8.5 years ago by WouterDeCoster 48k
1
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3.7k
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Comment: C: How to get human reference genome which is ready to use
8.5 years ago by WouterDeCoster 48k
2
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3.0k
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Comment: C: Interpreting Differentially Expressed Genes(DEGs) from RNA Seq experiment
8.5 years ago by WouterDeCoster 48k
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1.7k
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Comment: C: Subscription between genomic regions
8.5 years ago by WouterDeCoster 48k
2
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2.4k
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Answer: A: Question: combining RNAseq data from different platforms
8.5 years ago by WouterDeCoster 48k
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1
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1.7k
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Comment: C: Best splicing variant
8.5 years ago by WouterDeCoster 48k
0
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13k
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Comment: C: how to identify a sequencing sample's gender
8.5 years ago by WouterDeCoster 48k
1
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1
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3.1k
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Comment: C: Create gene expression matrix from miRNA
8.5 years ago by WouterDeCoster 48k
0
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1
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3.1k
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Comment: C: Create gene expression matrix from miRNA
8.5 years ago by WouterDeCoster 48k
1
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1.9k
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Answer: A: Retrieve header of column (field) in which data is above or equals a number
8.5 years ago by WouterDeCoster 48k
0
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0
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6.2k
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Comment: C: Please help me with pyfasta
8.5 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: Problems running the bam-readcount program: can NOT get started
8.5 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: Problems running the bam-readcount program: can NOT get started
8.5 years ago by WouterDeCoster 48k
0
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0
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19k
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Comment: C: Changing the record id in a FASTA file using BioPython
8.5 years ago by WouterDeCoster 48k
0
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0
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1.6k
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Comment: C: Extract bed file of deletions
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
0
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0
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2.9k
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Comment: C: popoolation parallelization problem
8.5 years ago by WouterDeCoster 48k
0
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1
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2.9k
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Comment: C: popoolation parallelization problem
8.5 years ago by WouterDeCoster 48k
0
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1
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2.4k
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Comment: C: python script modifications to get tabular output of blast from DEG(database of
8.5 years ago by WouterDeCoster 48k
0
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5.9k
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Comment: C: Output of featureCounts() is not integer
8.5 years ago by WouterDeCoster 48k
0
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0
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1.3k
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Answer: A: I need some sets of pathogenic variants related to any mendelian disorder.
8.5 years ago by WouterDeCoster 48k
0
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0
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4.2k
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Comment: C: how to extract a random set of SNP from a SNP table
8.5 years ago by WouterDeCoster 48k
0
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1
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4.2k
views
Comment: C: how to extract a random set of SNP from a SNP table
8.5 years ago by WouterDeCoster 48k
7,263 results • Page 82 of 146
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