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6
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1
reply
14k
views
Answer: A: Guessing The Quality Scale In Fastq Files
14.6 years ago by brentp 24k
1
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0
replies
10.0k
views
Comment: C: Rna-Seq Data Analysis & Good Review/Research Article On Same
14.7 years ago by brentp 24k
8
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1
reply
13k
views
Answer: A: Fasta Parser In C?
14.7 years ago by brentp 24k
4
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3
replies
11k
views
Answer: A: Fetching Read By Its Id From A Bam File With Pysam In Python
14.7 years ago by brentp 24k
0
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0
replies
105k
views
Comment: C: Selecting Random Pairs From Fastq?
14.7 years ago by brentp 24k
2
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1
reply
3.9k
views
Answer: A: Ucsc Browser And Novel Snps
14.7 years ago by brentp 24k
0
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0
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27k
views
Comment: C: Exon Coordinates Of Hg19 Genome Download
14.7 years ago by brentp 24k
11
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1
reply
6.6k
views
Answer: A: Tools & Techniques Bioinformatician Have To Master?
14.7 years ago by brentp 24k
0
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0
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27k
views
Comment: C: Exon Coordinates Of Hg19 Genome Download
14.7 years ago by brentp 24k
7
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0
replies
2.3k
views
Answer: A: What Are The Main Sources For Bioinformatic Software?
14.7 years ago by brentp 24k
0
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0
replies
18k
views
Comment: C: Extracting A Subset Of Sequences From A Fastq File (Biopython Speed)
14.7 years ago by brentp 24k
0
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0
replies
12k
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Comment: C: Degenerate Nucleotide Sequences
14.7 years ago by brentp 24k
0
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0
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11k
views
Comment: C: Anyone Know A *General* Variant (Snp/Indel) Effect Predictor / Annotator?
14.7 years ago by brentp 24k
0
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1
reply
4.8k
views
Answer: A: Simulate Paired-End Bisulfite Read Data
14.7 years ago by brentp 24k
0
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0
replies
6.0k
views
Comment: C: How To Run Bfast In Cluster Computing
14.7 years ago by brentp 24k
3
votes
0
replies
5.2k
views
Answer: A: Sequence Alignment Algorithm For Phred Phrap
14.7 years ago by brentp 24k
0
votes
0
replies
11k
views
Comment: C: Predicted Impact Of Indels?
14.8 years ago by brentp 24k
2
votes
0
replies
4.3k
views
Answer: A: Finding Distance Between Genes On Same Chromosome
14.8 years ago by brentp 24k
0
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0
replies
2.9k
views
Comment: C: Repeat Relationships In Gff3
14.8 years ago by brentp 24k
0
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0
replies
2.9k
views
Comment: C: Repeat Relationships In Gff3
14.8 years ago by brentp 24k
0
votes
0
replies
32k
views
Comment: C: Ngs - Huge (Fastq) File Parsing - Which Language For Good Efficiency ?
14.8 years ago by brentp 24k
0
votes
0
replies
14k
views
Comment: C: List All The Tools Or Write A Script To Validate That A Sequence Only Contains L
14.8 years ago by brentp 24k
3
votes
0
replies
6.9k
views
Answer: A: Snp Calling Tools And Costs
14.8 years ago by brentp 24k
7
votes
1
reply
8.7k
views
Answer: A: Conversion Of Solid Next Generation Sequencing Data
14.8 years ago by brentp 24k
2
votes
3
replies
18k
views
Answer: A: Installation Of Tophat -1.1.4
14.8 years ago by brentp 24k
2
votes
0
replies
10k
views
Answer: Answer: How Do We Discourage Ad-Hoc Bioinformatic Analyses?
updated 3.5 years ago by 45k • written 14.9 years ago by 24k
22
votes
2
replies
13k
views
Answer: A: The Best Question To Ask In A Bioinformatics Seminar
14.9 years ago by brentp 24k
1
vote
0
replies
7.4k
views
Comment: C: What Are Some Sanity Checks That Should Be Performed On Ngs Data?
14.9 years ago by brentp 24k
3
votes
1
reply
7.4k
views
Comment: C: What Are Some Sanity Checks That Should Be Performed On Ngs Data?
14.9 years ago by brentp 24k
1
vote
0
replies
7.4k
views
Comment: C: What Are Some Sanity Checks That Should Be Performed On Ngs Data?
14.9 years ago by brentp 24k
1
vote
0
replies
12k
views
Comment: C: Using Hdf5 To Store Bio-Data
15.0 years ago by brentp 24k
0
votes
0
replies
5.9k
views
Comment: C: Genomic Dna Hash Tables And Ambiguous Bases
15.0 years ago by brentp 24k
0
votes
0
replies
82k
views
Comment: C: How To Remove The Same Sequences In The Fasta Files?
15.0 years ago by brentp 24k
0
votes
0
replies
82k
views
Comment: C: How To Remove The Same Sequences In The Fasta Files?
15.0 years ago by brentp 24k
6
votes
0
replies
23k
views
Answer: A: How To Best Deal With Adapter Contamination (Illumina)?
15.0 years ago by brentp 24k
0
votes
0
replies
21k
views
Comment: C: I Am Preparing A Course On Ngs: Any Suggestion ?
15.0 years ago by brentp 24k
8
votes
4
replies
21k
views
Answer: A: I Am Preparing A Course On Ngs: Any Suggestion ?
15.0 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?
15.0 years ago by brentp 24k
0
votes
0
replies
3.1k
views
Comment: C: Statistics Advice
15.0 years ago by brentp 24k
0
votes
0
replies
5.7k
views
Comment: C: Snp Distribution On A Chromosome
15.0 years ago by brentp 24k
0
votes
0
replies
5.7k
views
Comment: C: Snp Distribution On A Chromosome
15.0 years ago by brentp 24k
0
votes
0
replies
9.7k
views
Comment: C: What License Do You Use When You Release Code And Data?
15.0 years ago by brentp 24k
3
votes
0
replies
23k
views
Answer: Answer: What Methods Do You Use For Short Read Mapping?
updated 2.1 years ago by 45k • written 15.7 years ago by 24k
0
votes
0
replies
13k
views
Comment: C: Best Spliced Aligner To Human Genome With Limited Rna-Seq Reads
15.0 years ago by brentp 24k
0
votes
0
replies
6.7k
views
Comment: C: How To Decide Whether To Keep: Het, U And Extra For Mapping Drosophila Genome
15.0 years ago by brentp 24k
4
votes
5
replies
6.7k
views
Answer: A: How To Decide Whether To Keep: Het, U And Extra For Mapping Drosophila Genome
15.0 years ago by brentp 24k
0
votes
0
replies
12k
views
Comment: C: Back Translating Protein Sequence Without Ambiguities...
15.1 years ago by brentp 24k
1
vote
0
replies
74k
views
Comment: C: What Tools/Libraries Do You Use To Visualize Genomic Feature Data?
15.1 years ago by brentp 24k
11
votes
2
replies
7.0k
views
Answer: A: Exponentially Increasing Genomes Slide
15.1 years ago by brentp 24k
0
votes
0
replies
72k
views
Comment: C: Python Script To Translate Rna Sequences To Protein Sequences
15.1 years ago by brentp 24k
916 results • Page 17 of 19
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