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1
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Comment: C: CNV detection using BAM file
7.7 years ago by WouterDeCoster 48k
1
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4.4k
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Answer: A: converting RSEM bam output into sam files for DEseq?
7.7 years ago by WouterDeCoster 48k
3
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4.4k
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Comment: C: converting RSEM bam output into sam files for DEseq?
7.7 years ago by WouterDeCoster 48k
0
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5.7k
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Comment: C: fastq to fasta conversion
7.7 years ago by WouterDeCoster 48k
1
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2.3k
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Comment: C: Having Issues with Variant Calling
7.7 years ago by WouterDeCoster 48k
1
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2
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2.8k
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Comment: C: Fastq header modification
7.7 years ago by WouterDeCoster 48k
0
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3.5k
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Comment: C: dbSNP Batch Query service will be discontinued June 2018: alternatives?
7.7 years ago by WouterDeCoster 48k
3
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3
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3.5k
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dbSNP Batch Query service will be discontinued June 2018: alternatives?
dbsnp
updated 7.7 years ago by 15k • written 7.7 years ago by 48k
2
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1
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1.2k
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Comment: C: Variation and Exon number
7.7 years ago by WouterDeCoster 48k
0
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0
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1.2k
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Comment: C: Tophat alignment error
7.7 years ago by WouterDeCoster 48k
0
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1
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13k
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Comment: C: how to extract/grep lines containing specific word?
7.7 years ago by WouterDeCoster 48k
1
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1
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2.7k
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Comment: C: Sanger validated SNP not present in IGV despite 10X coverage at site??!!
7.7 years ago by WouterDeCoster 48k
0
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1
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2.6k
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Comment: C: vcftools: unwanted filtering
7.7 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Comment: C: Fastq header modification
7.7 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Comment: C: Fastq header modification
7.7 years ago by WouterDeCoster 48k
0
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0
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9.8k
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Comment: C: enrichment of gene set with enrichR
7.7 years ago by WouterDeCoster 48k
0
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0
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5.0k
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Comment: C: Fastq files with integer instead of acii quality scores
7.7 years ago by WouterDeCoster 48k
0
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1
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2.6k
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Comment: C: How can I find the same record in two file? Use python
7.7 years ago by WouterDeCoster 48k
0
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0
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9.8k
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Comment: C: enrichment of gene set with enrichR
7.7 years ago by WouterDeCoster 48k
0
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0
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3.1k
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Comment: C: bim and fam downloaded as .txt files, won't work with PLINK?
7.7 years ago by WouterDeCoster 48k
3
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0
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9.8k
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Comment: C: enrichment of gene set with enrichR
7.7 years ago by WouterDeCoster 48k
0
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0
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6.9k
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Comment: C: Best way to trim PolyA in RNA Seq reads?
7.7 years ago by WouterDeCoster 48k
1
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2
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9.8k
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Comment: C: enrichment of gene set with enrichR
7.7 years ago by WouterDeCoster 48k
2
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1
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6.9k
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Answer: A: Best way to trim PolyA in RNA Seq reads?
7.7 years ago by WouterDeCoster 48k
1
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2
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6.9k
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Comment: C: Best way to trim PolyA in RNA Seq reads?
7.7 years ago by WouterDeCoster 48k
0
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1
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9.8k
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Comment: C: enrichment of gene set with enrichR
7.7 years ago by WouterDeCoster 48k
0
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1
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9.8k
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Comment: C: enrichment of gene set with enrichR
7.7 years ago by WouterDeCoster 48k
2
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0
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1.7k
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Comment: C: HELP ! COGS VALIDATION: GOOD ALIGNMENT??
7.7 years ago by WouterDeCoster 48k
1
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0
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5.0k
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Comment: C: Sorting my .bam with samtools produces differences in the fastq files generated
7.7 years ago by WouterDeCoster 48k
0
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0
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4.3k
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Comment: C: STAR aligned reads minimum maping quality
7.7 years ago by WouterDeCoster 48k
0
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0
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1.8k
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Comment: C: Reference genome version
7.7 years ago by WouterDeCoster 48k
0
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0
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3.6k
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Comment: C: Where I can download separate complete human chromosome genomes in GenBank forma
7.7 years ago by WouterDeCoster 48k
0
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0
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2.7k
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Comment: C: How to convert bam into fasta with chromosome name in fasta file
7.7 years ago by WouterDeCoster 48k
2
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1
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5.6k
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Comment: C: Haploview error(plz help)
7.7 years ago by WouterDeCoster 48k
0
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0
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2.3k
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Comment: C: How to further process and annotate VCF files derived from mapping a patient`s w
7.7 years ago by WouterDeCoster 48k
1
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1
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16k
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Answer: A: Modern software for whole genome alignment visualization
7.7 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: How to further process and annotate VCF files derived from mapping a patient`s w
7.7 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: How to further process and annotate VCF files derived from mapping a patient`s w
7.7 years ago by WouterDeCoster 48k
0
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1
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1.5k
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Comment: C: unable to login via github
7.7 years ago by WouterDeCoster 48k
2
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0
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1.4k
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Comment: C: Want Help regarding Text parsing.
7.7 years ago by WouterDeCoster 48k
0
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1
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4.7k
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Comment: C: Where to get >200Gb to build Bovine genome index in HISAT2?
7.7 years ago by WouterDeCoster 48k
0
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1
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4.7k
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Comment: C: Where to get >200Gb to build Bovine genome index in HISAT2?
7.7 years ago by WouterDeCoster 48k
0
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1
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4.7k
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Comment: C: Where to get >200Gb to build Bovine genome index in HISAT2?
7.7 years ago by WouterDeCoster 48k
0
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0
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4.7k
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Comment: C: Where to get >200Gb to build Bovine genome index in HISAT2?
7.7 years ago by WouterDeCoster 48k
0
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0
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4.7k
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Comment: C: Where to get >200Gb to build Bovine genome index in HISAT2?
7.7 years ago by WouterDeCoster 48k
1
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0
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1.7k
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Answer: A: Can splice-site mutations be treated as gene knock-outs?
7.7 years ago by WouterDeCoster 48k
0
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0
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1.9k
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Comment: C: how to deal with secondary alignment when calling snps
7.7 years ago by WouterDeCoster 48k
1
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0
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3.4k
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Comment: C: SNP calling in 2018
7.7 years ago by WouterDeCoster 48k
0
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0
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1.8k
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Comment: C: How many reads needed to be sure a variant does not exist?
7.7 years ago by WouterDeCoster 48k
2
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1
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1.8k
views
Comment: C: How many reads needed to be sure a variant does not exist?
7.7 years ago by WouterDeCoster 48k
7,263 results • Page 51 of 146
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