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Answer: A: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 3.9 years ago by 43k • written 11.5 years ago by ★ 3.6k
2
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0
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Answer: A: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 3.9 years ago by 43k • written 11.5 years ago by ★ 3.6k
11
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4
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Answer: A: Best Way To Merge A Many Thousand Small Bam Files Into One Big Bam File?
updated 4.3 years ago by 43k • written 12.8 years ago by ★ 3.6k
1
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1
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3.2k
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Answer: A: Perl Option For Mir Target Prediction?
updated 4.7 years ago by 43k • written 13.3 years ago by ★ 3.6k
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39k
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Answer: A: Extracting Sequence From A 3Gb Fasta File
updated 5.7 years ago by 43k • written 12.9 years ago by ★ 3.6k
2
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1
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9.2k
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Answer: A: TPM for ChIP-seq normalization
7.9 years ago by Ryan Thompson ★ 3.6k
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25k
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Answer: Answer: How to determine reference genome that was used for alignment given BAM with obs
updated 16 months ago by 43k • written 8.9 years ago by ★ 3.6k
1
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2
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9.1k
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Answer: A: What Are Numbers Every Bioinformatician Should Know?
10.7 years ago by Ryan Thompson ★ 3.6k
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4.0k
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Answer: A: Is There A Package To Map Primer Pair On Genome In R/Bioconductor?
10.7 years ago by Ryan Thompson ★ 3.6k
8
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8.2k
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Answer: A: Is Biostar Killing The Bioinformatics Core?
11.1 years ago by Ryan Thompson ★ 3.6k
1
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1
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18k
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Answer: A: Is It Possible To Generate A Sam Header Without Any External Header Information?
11.1 years ago by Ryan Thompson ★ 3.6k
2
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1
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2.3k
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Answer: A: Clustering Of Ncrna
11.1 years ago by Ryan Thompson ★ 3.6k
1
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0
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36k
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Answer: A: How To Determine If Paired–End Illumina Rnaseq Reads Are Strand–Specific
11.1 years ago by Ryan Thompson ★ 3.6k
3
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2
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6.2k
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Answer: A: Get Normalized Read Count Sample Matrix Tophat/Cufflinks
11.1 years ago by Ryan Thompson ★ 3.6k
3
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2
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5.9k
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Answer: A: What Is A Better Choice For Clustering Illumina Sequences Cd-Hit Or Uclust?
11.2 years ago by Ryan Thompson ★ 3.6k
1
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1
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7.9k
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Answer: A: Designing Command-Line Interfaces (Clis) For Scientific Software
11.2 years ago by Ryan Thompson ★ 3.6k
2
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1
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78k
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Answer: A: How Much Coverage Do We Need For An Rna-Seq Experiment?
11.2 years ago by Ryan Thompson ★ 3.6k
4
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1
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6.0k
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Answer: A: Coverage For Pair-End Rna-Seq, Extend Reads Or Not?
11.2 years ago by Ryan Thompson ★ 3.6k
2
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0
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17k
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Answer: A: Split Read Mapping By Bwa And Bowtie2
11.2 years ago by Ryan Thompson ★ 3.6k
3
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1
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7.4k
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Answer: A: How To Decide Which Genome Assembly Is Better?
11.2 years ago by Ryan Thompson ★ 3.6k
1
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1
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3.5k
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Answer: Answer: A Rank-Weighted Similarity Score
updated 2.1 years ago by 43k • written 11.3 years ago by ★ 3.6k
0
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0
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11k
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Answer: A: Sorting Fastq Files After Trimming (Orphans And Pe)
11.3 years ago by Ryan Thompson ★ 3.6k
1
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2
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3.9k
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Answer: A: Can Zram Be Used To Reduce The Hardware Requirements For De Novo Assembly?
11.3 years ago by Ryan Thompson ★ 3.6k
1
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0
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2.4k
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Answer: A: Limma - Special Case Of Contrasting
11.4 years ago by Ryan Thompson ★ 3.6k
0
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1
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2.2k
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Answer: A: Music Ports
11.5 years ago by Ryan Thompson ★ 3.6k
1
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0
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10k
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Answer: A: Count Junctions In A Sam/Bam File
11.5 years ago by Ryan Thompson ★ 3.6k
0
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0
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3.8k
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Answer: A: Cuffdiff - Doesn'T Appear To Be A Valid Bam File
11.6 years ago by Ryan Thompson ★ 3.6k
0
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0
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3.3k
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Answer: A: How Do I Deal Programmatically With Retired Ensembl Ids?
11.6 years ago by Ryan Thompson ★ 3.6k
39
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2
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44k
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Answer: A: Why Do You Need To Use Cdna For Rna-Seq?
11.6 years ago by Ryan Thompson ★ 3.6k
0
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1
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6.5k
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Answer: A: Identify Identical Sequences In Fastq File
11.7 years ago by Ryan Thompson ★ 3.6k
2
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0
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2.5k
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Answer: A: How To Resolve A Dispute Over Sequencing Data
11.7 years ago by Ryan Thompson ★ 3.6k
0
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0
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4.0k
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Answer: A: Retrieve Pairs Sequences By Id Form Sam Or Bam File
11.8 years ago by Ryan Thompson ★ 3.6k
0
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1
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4.0k
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Answer: A: Annotation In Gff3
11.9 years ago by Ryan Thompson ★ 3.6k
2
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0
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5.2k
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Answer: A: Can I Pre-Build The Shared Transcriptome Index For A Series Of Tophat Runs?
11.9 years ago by Ryan Thompson ★ 3.6k
2
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0
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2.5k
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Answer: A: How Many Chromosomes Have To Be Annotated For Human Beings?
11.9 years ago by Ryan Thompson ★ 3.6k
10
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0
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12k
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Answer: A: Sequencing And Strands
11.9 years ago by Ryan Thompson ★ 3.6k
2
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0
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3.3k
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Answer: A: What Is A "Coverage Island" In The Context Of Tophat?
11.9 years ago by Ryan Thompson ★ 3.6k
0
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0
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3.5k
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Answer: A: Cufflinks Or Cuffdiff (Or Both) For Frag-Bias-Correct?
12.0 years ago by Ryan Thompson ★ 3.6k
1
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0
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3.7k
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Answer: A: Get Snps, Indels From Biopython Blast Parser
12.0 years ago by Ryan Thompson ★ 3.6k
10
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1
reply
22k
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Answer: A: Blast Two Sequences
12.0 years ago by Ryan Thompson ★ 3.6k
2
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1
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2.0k
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Answer: A: Verifying Next Gen Seq Source
12.1 years ago by Ryan Thompson ★ 3.6k
1
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1
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6.4k
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Answer: A: Is It Necessary To Do Read Trimming For Rna-Seq Data?
12.1 years ago by Ryan Thompson ★ 3.6k
0
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0
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7.0k
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Answer: A: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.1 years ago by Ryan Thompson ★ 3.6k
5
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2
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10k
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Answer: A: Which Aligner Should I Use For Mapping Bacterial Rna-Seq Data
12.1 years ago by Ryan Thompson ★ 3.6k
0
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0
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4.3k
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Answer: A: Variable Length Reads In De Novo Assembly
12.8 years ago by Ryan Thompson ★ 3.6k
2
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0
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5.8k
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Answer: A: Snps In Promoter Regions In Exome Sequencing?
12.9 years ago by Ryan Thompson ★ 3.6k
9
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3
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12k
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Answer: Answer: Is There Any Reference Exome ?
updated 17 months ago by 43k • written 13.1 years ago by ★ 3.6k
2
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2
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13k
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Answer: A: Guessing The Quality Scale In Fastq Files
13.1 years ago by Ryan Thompson ★ 3.6k
3
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0
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24k
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Answer: A: Processing Fastq Files In R/Bioconductor Without Reading Entire Files Into Memor
13.2 years ago by Ryan Thompson ★ 3.6k
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