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Comment: C: IGV error: Error loading SAM header: For sequence 34711, text and binary have di
8.4 years ago by WouterDeCoster 48k
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1.6k
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Comment: C: Query about bioinformatics service
8.4 years ago by WouterDeCoster 48k
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1.6k
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Comment: C: Query about bioinformatics service
8.4 years ago by WouterDeCoster 48k
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1.6k
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Comment: C: Query about bioinformatics service
8.4 years ago by WouterDeCoster 48k
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Comment: C: Yet Another Programming Language
8.4 years ago by WouterDeCoster 48k
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6.3k
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Comment: C: Yet Another Programming Language
8.4 years ago by WouterDeCoster 48k
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2.7k
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Comment: C: cummeRbund error when loading cuffdiff data output
8.4 years ago by WouterDeCoster 48k
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6.3k
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Comment: C: Yet Another Programming Language
8.4 years ago by WouterDeCoster 48k
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4.3k
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Comment: C: Is there a more efficient way of checking multiple sequences for how many hits t
8.4 years ago by WouterDeCoster 48k
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7.8k
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Comment: C: Remove the last few bases from fasta sequences
8.4 years ago by WouterDeCoster 48k
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4.4k
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Comment: C: Splitting a fasta file on the basis of header barcodes
8.4 years ago by WouterDeCoster 48k
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1.6k
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Comment: C: Using long reads to find a combination of mutations
8.4 years ago by WouterDeCoster 48k
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2.3k
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Comment: C: how can I keep only those SNP in file "a" which match to SNPs in file "b"?
8.4 years ago by WouterDeCoster 48k
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3.9k
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Answer: C: number of threads for cufflinks transcript assembly
8.4 years ago by WouterDeCoster 48k
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18k
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Comment: C: download sequences form ncbi using python
8.4 years ago by WouterDeCoster 48k
0
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1
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7.8k
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Comment: C: Remove the last few bases from fasta sequences
8.4 years ago by WouterDeCoster 48k
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0
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7.4k
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Comment: C: problem with chromosomes in michigan imputation server
8.4 years ago by WouterDeCoster 48k
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0
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18k
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Comment: C: download sequences form ncbi using python
8.4 years ago by WouterDeCoster 48k
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1.7k
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Comment: C: the content of FAST5 files that are generated from Poretools Events
8.4 years ago by WouterDeCoster 48k
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1
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2.8k
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Comment: C: Lack of early variants
8.4 years ago by WouterDeCoster 48k
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2.3k
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Comment: C: Help with R studio
8.4 years ago by WouterDeCoster 48k
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0
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2.3k
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Comment: C: Help with R studio
8.4 years ago by WouterDeCoster 48k
1
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1
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2.3k
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Comment: C: Help with R studio
8.4 years ago by WouterDeCoster 48k
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2
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2.3k
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Comment: C: Help with R studio
8.4 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: Help with R studio
8.4 years ago by WouterDeCoster 48k
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0
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2.3k
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Comment: C: Help with R studio
8.4 years ago by WouterDeCoster 48k
0
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1
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6.3k
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Comment: C: Error with atomtypes in gromacs
8.4 years ago by WouterDeCoster 48k
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1.6k
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Comment: C: Labs with bioinformatics courses mainly focussing on Next generation sequence da
8.4 years ago by WouterDeCoster 48k
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4.0k
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Comment: C: The Biostar Handbook: A Beginner's Guide to Bioinformatics
8.4 years ago by WouterDeCoster 48k
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1
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7.3k
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Comment: C: What the heck is going on with this DESeq2 MA Plot?
8.4 years ago by WouterDeCoster 48k
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3.3k
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Comment: C: bowtie: poor mapping with high quality reads
8.4 years ago by WouterDeCoster 48k
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3.6k
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Comment: C: chromosomal locations of telomeric regions from the Genome
8.4 years ago by WouterDeCoster 48k
2
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1
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3.7k
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Comment: C: what is different between principle applied between tophat2 and hisat2?
8.4 years ago by WouterDeCoster 48k
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1
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1.8k
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Comment: C: How to separate small RNA reads that show 10nt overlap?
8.4 years ago by WouterDeCoster 48k
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3.0k
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Comment: C: how to select certain columns in R
8.4 years ago by WouterDeCoster 48k
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3.0k
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Comment: C: how to select certain columns in R
8.4 years ago by WouterDeCoster 48k
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0
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3.0k
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Comment: C: how to analyze CNV "copy number variation" data
8.4 years ago by WouterDeCoster 48k
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3.0k
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Comment: C: how to analyze CNV "copy number variation" data
8.4 years ago by WouterDeCoster 48k
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0
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2.7k
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Comment: C: RNAseq, Noise , Signal
8.4 years ago by WouterDeCoster 48k
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0
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3.1k
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Comment: C: Publicly-available disease genome VCF
8.4 years ago by WouterDeCoster 48k
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0
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2.2k
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Comment: C: RNAseq, poly(A) selection
8.4 years ago by WouterDeCoster 48k
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2.0k
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Comment: C: CONTRA baseline ZeroDivisionError: float division by zero
8.4 years ago by WouterDeCoster 48k
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0
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2.1k
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Comment: C: customize reference genome
8.4 years ago by WouterDeCoster 48k
1
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2
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2.6k
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Comment: C: ERROR USING BWASW (BWA 0.7.15-r1140): bwtsw2_pair.c line 122: failed to alloca
8.4 years ago by WouterDeCoster 48k
1
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0
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4.2k
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Comment: C: STAR Aligner Suddently changed output file???
8.4 years ago by WouterDeCoster 48k
1
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0
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4.2k
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Comment: C: STAR Aligner Suddently changed output file???
8.4 years ago by WouterDeCoster 48k
0
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0
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1.4k
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Comment: C: Python error for variant call
8.4 years ago by WouterDeCoster 48k
0
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0
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1.9k
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Comment: C: Bionformatics training courses and workshops in Europa?
8.4 years ago by WouterDeCoster 48k
2
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1.8k
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Comment: C: Can't we proceed with a SAM file for downstream RNA-Seq data analysis?
8.4 years ago by WouterDeCoster 48k
0
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1
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1.9k
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Answer: A: Bionformatics training courses and workshops in Europa?
8.4 years ago by WouterDeCoster 48k
7,263 results • Page 74 of 146
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