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6
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1
reply
14k
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Answer: A: Guessing The Quality Scale In Fastq Files
14.5 years ago by brentp 24k
1
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0
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9.7k
views
Comment: C: Rna-Seq Data Analysis & Good Review/Research Article On Same
14.5 years ago by brentp 24k
8
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1
reply
13k
views
Answer: A: Fasta Parser In C?
14.5 years ago by brentp 24k
4
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3
replies
11k
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Answer: A: Fetching Read By Its Id From A Bam File With Pysam In Python
14.5 years ago by brentp 24k
0
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0
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102k
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Comment: C: Selecting Random Pairs From Fastq?
14.5 years ago by brentp 24k
2
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1
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3.8k
views
Answer: A: Ucsc Browser And Novel Snps
14.5 years ago by brentp 24k
0
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0
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26k
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Comment: C: Exon Coordinates Of Hg19 Genome Download
14.5 years ago by brentp 24k
11
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1
reply
6.3k
views
Answer: A: Tools & Techniques Bioinformatician Have To Master?
14.5 years ago by brentp 24k
0
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0
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26k
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Comment: C: Exon Coordinates Of Hg19 Genome Download
14.5 years ago by brentp 24k
7
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0
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2.3k
views
Answer: A: What Are The Main Sources For Bioinformatic Software?
14.5 years ago by brentp 24k
0
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0
replies
17k
views
Comment: C: Extracting A Subset Of Sequences From A Fastq File (Biopython Speed)
14.5 years ago by brentp 24k
0
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0
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12k
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Comment: C: Degenerate Nucleotide Sequences
14.5 years ago by brentp 24k
0
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0
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10k
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Comment: C: Anyone Know A *General* Variant (Snp/Indel) Effect Predictor / Annotator?
14.5 years ago by brentp 24k
0
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1
reply
4.6k
views
Answer: A: Simulate Paired-End Bisulfite Read Data
14.5 years ago by brentp 24k
0
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0
replies
5.9k
views
Comment: C: How To Run Bfast In Cluster Computing
14.5 years ago by brentp 24k
3
votes
0
replies
5.0k
views
Answer: A: Sequence Alignment Algorithm For Phred Phrap
14.6 years ago by brentp 24k
0
votes
0
replies
10k
views
Comment: C: Predicted Impact Of Indels?
14.6 years ago by brentp 24k
2
votes
0
replies
4.2k
views
Answer: A: Finding Distance Between Genes On Same Chromosome
14.6 years ago by brentp 24k
0
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0
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2.8k
views
Comment: C: Repeat Relationships In Gff3
14.6 years ago by brentp 24k
0
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0
replies
2.8k
views
Comment: C: Repeat Relationships In Gff3
14.6 years ago by brentp 24k
0
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0
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31k
views
Comment: C: Ngs - Huge (Fastq) File Parsing - Which Language For Good Efficiency ?
14.6 years ago by brentp 24k
0
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0
replies
13k
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Comment: C: List All The Tools Or Write A Script To Validate That A Sequence Only Contains L
14.6 years ago by brentp 24k
3
votes
0
replies
6.8k
views
Answer: A: Snp Calling Tools And Costs
14.6 years ago by brentp 24k
7
votes
1
reply
8.5k
views
Answer: A: Conversion Of Solid Next Generation Sequencing Data
14.7 years ago by brentp 24k
2
votes
3
replies
18k
views
Answer: A: Installation Of Tophat -1.1.4
14.7 years ago by brentp 24k
2
votes
0
replies
9.8k
views
Answer: Answer: How Do We Discourage Ad-Hoc Bioinformatic Analyses?
updated 3.4 years ago by 45k • written 14.7 years ago by 24k
22
votes
2
replies
13k
views
Answer: A: The Best Question To Ask In A Bioinformatics Seminar
14.7 years ago by brentp 24k
1
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0
replies
7.1k
views
Comment: C: What Are Some Sanity Checks That Should Be Performed On Ngs Data?
14.7 years ago by brentp 24k
3
votes
1
reply
7.1k
views
Comment: C: What Are Some Sanity Checks That Should Be Performed On Ngs Data?
14.7 years ago by brentp 24k
1
vote
0
replies
7.1k
views
Comment: C: What Are Some Sanity Checks That Should Be Performed On Ngs Data?
14.7 years ago by brentp 24k
1
vote
0
replies
12k
views
Comment: C: Using Hdf5 To Store Bio-Data
14.8 years ago by brentp 24k
0
votes
0
replies
5.7k
views
Comment: C: Genomic Dna Hash Tables And Ambiguous Bases
14.8 years ago by brentp 24k
0
votes
0
replies
80k
views
Comment: C: How To Remove The Same Sequences In The Fasta Files?
14.8 years ago by brentp 24k
0
votes
0
replies
80k
views
Comment: C: How To Remove The Same Sequences In The Fasta Files?
14.8 years ago by brentp 24k
6
votes
0
replies
22k
views
Answer: A: How To Best Deal With Adapter Contamination (Illumina)?
14.8 years ago by brentp 24k
0
votes
0
replies
20k
views
Comment: C: I Am Preparing A Course On Ngs: Any Suggestion ?
14.9 years ago by brentp 24k
8
votes
4
replies
20k
views
Answer: A: I Am Preparing A Course On Ngs: Any Suggestion ?
14.9 years ago by brentp 24k
0
votes
0
replies
19k
views
Comment: C: Should Samtools Pileup Be Performed On Uniquely Mapped Reads Or All The Reads?
14.9 years ago by brentp 24k
0
votes
0
replies
2.9k
views
Comment: C: Statistics Advice
14.9 years ago by brentp 24k
0
votes
0
replies
5.4k
views
Comment: C: Snp Distribution On A Chromosome
14.9 years ago by brentp 24k
0
votes
0
replies
5.4k
views
Comment: C: Snp Distribution On A Chromosome
14.9 years ago by brentp 24k
0
votes
0
replies
9.4k
views
Comment: C: What License Do You Use When You Release Code And Data?
14.9 years ago by brentp 24k
3
votes
0
replies
22k
views
Answer: Answer: What Methods Do You Use For Short Read Mapping?
updated 23 months ago by 45k • written 15.5 years ago by 24k
0
votes
0
replies
13k
views
Comment: C: Best Spliced Aligner To Human Genome With Limited Rna-Seq Reads
14.9 years ago by brentp 24k
0
votes
0
replies
6.6k
views
Comment: C: How To Decide Whether To Keep: Het, U And Extra For Mapping Drosophila Genome
14.9 years ago by brentp 24k
4
votes
5
replies
6.6k
views
Answer: A: How To Decide Whether To Keep: Het, U And Extra For Mapping Drosophila Genome
14.9 years ago by brentp 24k
0
votes
0
replies
11k
views
Comment: C: Back Translating Protein Sequence Without Ambiguities...
14.9 years ago by brentp 24k
1
vote
0
replies
73k
views
Comment: C: What Tools/Libraries Do You Use To Visualize Genomic Feature Data?
14.9 years ago by brentp 24k
11
votes
2
replies
6.7k
views
Answer: A: Exponentially Increasing Genomes Slide
14.9 years ago by brentp 24k
0
votes
0
replies
71k
views
Comment: C: Python Script To Translate Rna Sequences To Protein Sequences
14.9 years ago by brentp 24k
916 results • Page 17 of 19
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