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Comment: C: Cross-Posting To Here And Email Lists
14.3 years ago by Sean Davis 27k
3
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2.8k
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Comment: C: Redundancy Removal
14.3 years ago by Sean Davis 27k
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2.6k
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Comment: C: Sequence Analysis Software
14.3 years ago by Sean Davis 27k
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2
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2.6k
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Answer: A: Sequence Analysis Software
14.3 years ago by Sean Davis 27k
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2.6k
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Comment: C: Sequence Analysis Software
14.3 years ago by Sean Davis 27k
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3.3k
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Comment: C: Samtools Indels -- Filtering Only Hits With Insertion In The Reference In The Mi
14.3 years ago by Sean Davis 27k
3
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2
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4.6k
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Answer: A: Text Mining Tool For Gwas Papers
14.3 years ago by Sean Davis 27k
3
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0
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24k
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Answer: A: Mapping Genes To Pathway
14.3 years ago by Sean Davis 27k
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3.3k
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Comment: C: Samtools Indels -- Filtering Only Hits With Insertion In The Reference In The Mi
14.3 years ago by Sean Davis 27k
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3.4k
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Comment: C: Annovar And String Problems
14.3 years ago by Sean Davis 27k
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3.1k
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Answer: A: Analysing Multiple Exome Datasets
14.3 years ago by Sean Davis 27k
4
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1
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10k
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Answer: A: How Many Pass-Filter Reads Should I Expect From An Illumina Gaii Run?
14.3 years ago by Sean Davis 27k
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6.6k
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Comment: C: Aligning Mate Pair Data
14.3 years ago by Sean Davis 27k
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2
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6.6k
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Answer: A: Aligning Mate Pair Data
14.3 years ago by Sean Davis 27k
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6.9k
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Comment: C: What Does This Cigar Mean?
14.3 years ago by Sean Davis 27k
3
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5
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6.9k
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Answer: A: What Does This Cigar Mean?
14.3 years ago by Sean Davis 27k
1
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2.1k
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Answer: A: Incremental Additions To An Indexed Bam File?
14.3 years ago by Sean Davis 27k
2
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0
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2.2k
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Answer: A: New Pileup Output
14.3 years ago by Sean Davis 27k
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1
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8.3k
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Answer: A: Run Hundreds Of Bwa Commands Without Waiting
14.3 years ago by Sean Davis 27k
1
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0
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4.3k
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Comment: C: Chip-Seq Peak Caller Able To Find Peaks Split By Indels?
14.3 years ago by Sean Davis 27k
1
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0
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4.3k
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Answer: A: Chip-Seq Peak Caller Able To Find Peaks Split By Indels?
14.3 years ago by Sean Davis 27k
2
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0
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3.6k
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Answer: A: Detecting And Maping Balanced Translocations With Whole Genome Sequencing?
14.3 years ago by Sean Davis 27k
1
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0
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4.3k
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Comment: C: Chip-Seq Peak Caller Able To Find Peaks Split By Indels?
14.3 years ago by Sean Davis 27k
3
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3.4k
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Comment: C: Galaxy- Combining 2 Queries
14.3 years ago by Sean Davis 27k
4
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1
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4.6k
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Answer: A: Varscan Somatic...Syntax To Run With Redirect?
14.3 years ago by Sean Davis 27k
1
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0
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9.8k
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Comment: C: Pathway Analysis For List Of Genes
14.3 years ago by Sean Davis 27k
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5.2k
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Comment: C: Pysam Snp Calling
14.3 years ago by Sean Davis 27k
2
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2
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5.2k
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Answer: A: Pysam Snp Calling
14.3 years ago by Sean Davis 27k
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0
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2.8k
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Comment: C: .Gr Format From Rna-Seq
14.3 years ago by Sean Davis 27k
3
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2
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6.2k
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Answer: A: Copy Number Variation Tools For Illumina Hiseq Paired End Data (Whole Genome)?
14.3 years ago by Sean Davis 27k
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0
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6.2k
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Comment: C: Copy Number Variation Tools For Illumina Hiseq Paired End Data (Whole Genome)?
14.3 years ago by Sean Davis 27k
2
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0
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4.0k
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Answer: A: Feature Selection For Regression
14.3 years ago by Sean Davis 27k
0
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0
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7.5k
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Comment: Comment: Has Anyone Had Experience With Complete Genomics Sequencing And Data Analysis?
updated 4.5 years ago by 45k • written 14.4 years ago by 27k
0
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1
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3.4k
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Answer: A: Tools For Large Indels Discovery In Single-End Rna-Seq Reads
14.4 years ago by Sean Davis 27k
3
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2
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7.5k
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Answer: Answer: Has Anyone Had Experience With Complete Genomics Sequencing And Data Analysis?
updated 4.5 years ago by 45k • written 14.4 years ago by 27k
0
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0
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10k
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Comment: C: Illlumina Paired End Reads File Format
14.4 years ago by Sean Davis 27k
1
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0
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5.0k
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Comment: C: Bwa Aln For Snp/Indel Discovery With Paired End 100Bp Human Dna Reads
14.4 years ago by Sean Davis 27k
3
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5
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10k
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Answer: A: Illlumina Paired End Reads File Format
14.4 years ago by Sean Davis 27k
1
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0
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2.4k
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Answer: A: Fragile-X Bioinformatics Project
14.4 years ago by Sean Davis 27k
2
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0
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2.4k
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Comment: C: Fragile-X Bioinformatics Project
14.4 years ago by Sean Davis 27k
3
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0
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14k
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Comment: C: Massive Pairwise Comparison Using Biopython
14.4 years ago by Sean Davis 27k
0
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0
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4.2k
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Comment: C: Need: Working Workflow Pipeline For Agilent Mirna Analysis Using Agimicrorna
14.4 years ago by Sean Davis 27k
0
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0
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5.7k
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Comment: C: Varscan Error In Pileup2Snp
14.4 years ago by Sean Davis 27k
3
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0
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3.1k
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Answer: A: Snp Association Next Gen Sequencing
14.4 years ago by Sean Davis 27k
3
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0
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6.3k
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Answer: A: Loh Analysis Of Ngs(Exome) Data
14.4 years ago by Sean Davis 27k
3
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1
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11k
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Answer: A: Peak Detection In Intergenic Regions In Rna-Seq Data
14.5 years ago by Sean Davis 27k
2
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0
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3.7k
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Comment: C: Detection Of Cnvs From Targeted Resequencing Experiments
14.5 years ago by Sean Davis 27k
1
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1
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3.6k
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Answer: A: Human Transcriptome Annotations?
14.6 years ago by Sean Davis 27k
0
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0
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6.0k
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Comment: C: What Is The Typical Density Of Heterozygous Alleles In A Diploid Human Genome?
14.6 years ago by Sean Davis 27k
0
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0
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6.0k
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Answer: A: What Is The Typical Density Of Heterozygous Alleles In A Diploid Human Genome?
14.6 years ago by Sean Davis 27k
1,985 results • Page 39 of 40
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