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3
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1
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5.5k
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Answer: A: Add data to Vcf Info Field
11.2 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.4k
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Answer: A: predictCoding function in VariantAnnotation packages
11.2 years ago Valerie Obenchain ★ 6.8k
1
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0
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1.4k
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Answer: A: trigger package fails at parallalization - Transcriptional Regulatory Inference
11.2 years ago Valerie Obenchain ★ 6.8k
2
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0
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1.7k
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Answer: A: Missing KRAS in locateVariants or TxDb.Hsapiens.UCSC.hg19.knownGene?
11.2 years ago Valerie Obenchain ★ 6.8k
5
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0
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1.4k
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News: October Newsletter now available
newsletter News
11.2 years ago Valerie Obenchain ★ 6.8k
1
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0
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2.3k
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Answer: A: 'seqlevels(seqinfo(x))' and 'levels(seqnames(x))' are not identical
11.3 years ago Valerie Obenchain ★ 6.8k
3
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0
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1.8k
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Answer: A: Bioinformatics researching Schizophrenia
updated 11.3 years ago by 25k • written 11.3 years ago by ★ 6.8k
0
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0
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2.3k
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Comment: C: nearly exact overlaps between GAlignmentPairs and GenomicRanges
11.4 years ago Valerie Obenchain ★ 6.8k
0
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0
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2.5k
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Answer: A: narrow and xstringset
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.8k
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Comment: C: iranges
11.4 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.1k
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Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
VariantAnnotation Annotation GenomicRanges VariantAnnotation GenomicAlignments Annotation
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.8k
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Answer: A: iranges
11.4 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.8k
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Comment: C: iranges
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.8k
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Answer: A: iranges
11.4 years ago Valerie Obenchain ★ 6.8k
0
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0
replies
855
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Comment: C: Question about Rle
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
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855
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Answer: A: Question about Rle
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
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2.3k
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Answer: A: DNACopy Question what is passed to the maploc argument.
11.4 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.1k
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Answer: A: Error in getting exons sequence
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
reply
1.7k
views
Comment: C: Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
reply
1.7k
views
Comment: C: Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
11.4 years ago Valerie Obenchain ★ 6.8k
0
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5
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1.7k
views
Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
VariantAnnotation GenomicRanges VariantAnnotation VariantAnnotation GenomicRanges
updated 11.4 years ago by ★ 3.4k • written 11.5 years ago by ★ 6.8k
0
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1
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6.1k
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Comment: C: Linkage disequilibrium with 1000 Genomes/HapMap
11.4 years ago Valerie Obenchain ★ 6.8k
0
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1
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3.6k
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Comment: C: GenomicAlignments - Speeding up readGAlignmentPairs()
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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3.6k
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Comment: C: GenomicAlignments - Speeding up readGAlignmentPairs()
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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3.6k
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Comment: C: GenomicAlignments - Speeding up readGAlignmentPairs()
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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3.6k
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Comment: C: GenomicAlignments - Speeding up readGAlignmentPairs()
11.5 years ago Valerie Obenchain ★ 6.8k
0
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10
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3.6k
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GenomicAlignments - Speeding up readGAlignmentPairs()
Cancer RNAseqData GenomicFeatures Cancer RNAseqData GenomicFeatures
updated 11.5 years ago by ▴ 320 • written 11.5 years ago by ★ 6.8k
0
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0
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699
views
Bioconductor newsletter - July 2014
Cancer Cancer
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.6k
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Comment: C: Using GenomicAlignments to get Exon-centric Counts
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.6k
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Answer: A: Using GenomicAlignments to get Exon-centric Counts
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.2k
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Comment: C: apply function on genomicsRanges ob
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.2k
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Answer: A: apply function on genomicsRanges ob
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.7k
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Answer: A: DNAStringSet_translate error in predictCoding()
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.9k
views
Comment: C: second GenomicRanges request - enable query-self comparison (and so ignoreSelf a
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.7k
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Answer: A: DNAStringSet_translate error in predictCoding()
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
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1.9k
views
Comment: C: second GenomicRanges request - enable query-self comparison (and so ignoreSelf a
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
replies
2.3k
views
Answer: A: mutant allele read counts
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
reply
2.3k
views
Answer: A: mutant allele read counts
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
reply
1.9k
views
Comment: C: second GenomicRanges request - enable query-self comparison (and so ignoreSelf a
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
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2.3k
views
Answer: A: mutant allele read counts
11.5 years ago Valerie Obenchain ★ 6.8k
0
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1
reply
2.3k
views
Answer: A: mutant allele read counts
11.5 years ago Valerie Obenchain ★ 6.8k
1
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1
reply
4.7k
views
Answer: A: readGappedAlignments not working in Rsamtools
11.5 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.3k
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Comment: C: VCF class: different length when unlisting INFO CompressedCharacterList
11.6 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.9k
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Comment: C: GenomicAlignments and QNAME collision
11.6 years ago Valerie Obenchain ★ 6.8k
0
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4
replies
1.9k
views
GenomicAlignments and QNAME collision
RNASeq Cancer convert Rsamtools GenomicAlignments RNASeq Cancer convert Rsamtools
updated 11.6 years ago by ▴ 90 • written 11.6 years ago by ★ 6.8k
0
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1
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1.9k
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Comment: C: GenomicAlignments and QNAME collision
11.6 years ago Valerie Obenchain ★ 6.8k
0
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0
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1.7k
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Comment: C: GenomicAlignments and QNAME collision
11.6 years ago Valerie Obenchain ★ 6.8k
0
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0
replies
1.4k
views
Answer: A: VCF class: different length when unlisting INFO CompressedCharacterList
11.6 years ago Valerie Obenchain ★ 6.8k
0
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1
reply
1.1k
views
Answer: A: readGAlignmentPairs perfromace issue
11.6 years ago Valerie Obenchain ★ 6.8k
0
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0
replies
4.1k
views
Answer: A: Multi-sample VCF file and filterVcf
11.6 years ago Valerie Obenchain ★ 6.8k
830 results • Page 9 of 17
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