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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.5 years ago by 44k • written 12.4 years ago by 3.9k
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1
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67k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.5 years ago by 44k • written 12.4 years ago by 3.9k
0
votes
1
reply
67k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
updated 4.5 years ago by 44k • written 12.4 years ago by 3.9k
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0
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20k
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Comment: C: Use Tabix With A List Of Regions
updated 5.2 years ago by 44k • written 10.1 years ago by 3.9k
3
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11k
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Comment: C: Thoughts On Galaxy For Next Generation Sequence Data Analysis
updated 5.2 years ago by 44k • written 13.4 years ago by 3.9k
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5.3k
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Comment: A: elPrep 4.0.0, a high-performance drop-in replacement tool for GATK4/Picard/SAMto
6.1 years ago by Leonor Palmeira 3.9k
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5.3k
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Comment: C: elPrep 4.0.0, a high-performance drop-in replacement tool for GATK4/Picard/SAMto
6.1 years ago by Leonor Palmeira 3.9k
2
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1
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5.3k
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Comment: C: elPrep 4.0.0, a high-performance drop-in replacement tool for GATK4/Picard/SAMto
6.1 years ago by Leonor Palmeira 3.9k
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2.4k
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Comment: C: BamUtil for Base Qual Recalibration
7.6 years ago by Leonor Palmeira 3.9k
0
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2
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15k
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Comment: Comment: Retrieve Subset Positions Vcf File
updated 2.8 years ago by 44k • written 10.1 years ago by 3.9k
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1
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15k
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Comment: C: Retrieve Subset Positions Vcf File
10.1 years ago by Leonor Palmeira 3.9k
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2.9k
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Comment: Comment: Author affiliation and for-profit licensing of published software
updated 2.9 years ago by 44k • written 10.1 years ago by 3.9k
2
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0
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17k
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Comment: C: Gatk - Haplotypecaller Is So Slow, What Is Faster And As Good?
10.1 years ago by Leonor Palmeira 3.9k
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31k
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Comment: C: Amino Acid Change To Genomic Location
10.1 years ago by Leonor Palmeira 3.9k
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14k
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Comment: C: Is there a tool to transform GenomeStudio genotype format to VCF?
10.4 years ago by Leonor Palmeira 3.9k
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0
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14k
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Comment: C: Is there a tool to transform GenomeStudio genotype format to VCF?
10.5 years ago by Leonor Palmeira 3.9k
0
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1
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14k
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Comment: C: CNV analysis tool on exome data for NGS
10.6 years ago by Leonor Palmeira 3.9k
1
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0
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24k
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Comment: C: Downsampling Bam Files
10.6 years ago by Leonor Palmeira 3.9k
7
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1
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50k
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Comment: C: Fastq Splitter For Paired End Reads
10.7 years ago by Leonor Palmeira 3.9k
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3.7k
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Comment: C: Ngs Course Medical Genomics, Leuven, 17-20 September 2013
11.2 years ago by Leonor Palmeira 3.9k
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0
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3.7k
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Comment: C: Ngs Course Medical Genomics, Leuven, 17-20 September 2013
11.3 years ago by Leonor Palmeira 3.9k
1
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0
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65k
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Comment: C: Recommended Tools For Alternative Splicing Detection From Rna-Seq Data
11.3 years ago by Leonor Palmeira 3.9k
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6.7k
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Comment: C: Detecting Chimeric Transcripts In Rna-Seq De Novo Assemblies
11.3 years ago by Leonor Palmeira 3.9k
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2
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3.7k
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Comment: C: Ngs Course Medical Genomics, Leuven, 17-20 September 2013
11.4 years ago by Leonor Palmeira 3.9k
5
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1
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6.8k
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Comment: C: Converting Gene Predictions In Glimmer To Protein Sequences.
11.4 years ago by Leonor Palmeira 3.9k
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2
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6.3k
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Comment: C: How Can I Convert Novoalign Output Format To Sam Or Bam?
11.4 years ago by Leonor Palmeira 3.9k
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0
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14k
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Comment: C: Comparison Of Soap And Bwa
11.4 years ago by Leonor Palmeira 3.9k
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0
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2.5k
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Comment: C: Mira Tcs Output Currently Not Available
11.9 years ago by Leonor Palmeira 3.9k
1
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0
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4.2k
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Comment: C: Is It Possible To Find Sample Batch # In Cel Files?
11.9 years ago by Leonor Palmeira 3.9k
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0
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3.0k
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Comment: C: How To Remove Macrophage Contamination From A Rna-Seq Experiment?
11.9 years ago by Leonor Palmeira 3.9k
2
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1
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8.4k
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Comment: C: State Of Biostar - Future Directions (January 2013)
11.9 years ago by Leonor Palmeira 3.9k
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3.8k
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Comment: C: Counting Instances Of "No Overlap"
12.1 years ago by Leonor Palmeira 3.9k
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0
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4.7k
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Comment: C: How To Calculate Number Of Gap Windows And Their Length In A Multiple Alignment
12.3 years ago by Leonor Palmeira 3.9k
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2
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3.6k
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Comment: C: Where Is Pam 1.0.7 Source (To Generate Pam Substitution Matrices)?
12.3 years ago by Leonor Palmeira 3.9k
0
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1
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7.9k
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Comment: C: Non-Transcribed Strand And Transcribed Strand Mutations In Sequencing
12.4 years ago by Leonor Palmeira 3.9k
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2
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7.9k
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Comment: C: Non-Transcribed Strand And Transcribed Strand Mutations In Sequencing
12.4 years ago by Leonor Palmeira 3.9k
1
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0
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11k
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Comment: C: How Much Does It Cost To Align A Flowcell In The Cloud?
12.4 years ago by Leonor Palmeira 3.9k
0
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1
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11k
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Comment: C: How Much Does It Cost To Align A Flowcell In The Cloud?
12.4 years ago by Leonor Palmeira 3.9k
0
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0
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3.2k
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Comment: C: Phylogenetic Tree Using Numts
12.4 years ago by Leonor Palmeira 3.9k
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3.2k
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Comment: C: Phylogenetic Tree Using Numts
12.4 years ago by Leonor Palmeira 3.9k
0
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2
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3.2k
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Comment: C: Phylogenetic Tree Using Numts
12.4 years ago by Leonor Palmeira 3.9k
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2
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3.2k
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Comment: C: Phylogenetic Tree Using Numts
12.4 years ago by Leonor Palmeira 3.9k
0
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0
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7.8k
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Comment: C: Conversion Of Solid Next Generation Sequencing Data
12.4 years ago by Leonor Palmeira 3.9k
0
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1
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5.2k
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Comment: C: Scripts Calculate Tetranuclear Frequency
12.4 years ago by Leonor Palmeira 3.9k
0
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0
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3.7k
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Comment: C: Reading Cgh Arrays Data Into R
12.4 years ago by Leonor Palmeira 3.9k
0
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1
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5.2k
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Comment: C: Scripts Calculate Tetranuclear Frequency
12.4 years ago by Leonor Palmeira 3.9k
0
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0
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4.3k
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Comment: C: How To Deal With Multiple Transcription Start Sites [Refseq || Chipseq]
12.4 years ago by Leonor Palmeira 3.9k
0
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0
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6.9k
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Comment: C: Cummerbund
12.4 years ago by Leonor Palmeira 3.9k
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0
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31k
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Comment: C: Filtering Fasta Sequences By Chromosomes Names From A Big Fasta File
12.4 years ago by Leonor Palmeira 3.9k
0
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0
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13k
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Comment: C: How To Get The Clear Values At The Bottom Of A Dendrogram In Clustering In R?
12.4 years ago by Leonor Palmeira 3.9k
157 results • Page 1 of 4
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