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2
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Answer: A: Is It Possible To Use And Cite Ncbi Geo Datasets That Don'T Have A Already-Publi
11.1 years ago by Ian 6.1k
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4.7k
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Comment: C: Is It Okay To Remove Chrun And Chr*_Random Reads From A Bed File?
11.1 years ago by Ian 6.1k
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12k
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Answer: A: Tool Recommendation Wanted For Cleaning Fasta/Fastq Files To Remove Unpaired Rea
11.1 years ago by Ian 6.1k
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0
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2.0k
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Answer: A: Integrating Genome Tracks Inside A Web Page
11.1 years ago by Ian 6.1k
1
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6.3k
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Answer: A: Tool Or Technique To Find Co-Occuring Motifs Within Genomic Intervals That Corr
11.2 years ago by Ian 6.1k
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3.3k
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Comment: C: Tool For Binning Windowbed Output For K-Means Clustering
11.2 years ago by Ian 6.1k
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4.4k
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Comment: C: K-Means Clustering
11.2 years ago by Ian 6.1k
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3.7k
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Answer: A: Confused With Peaks And Motifs
11.2 years ago by Ian 6.1k
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3.9k
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Answer: A: About Mouse Reference Genome
11.2 years ago by Ian 6.1k
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2.8k
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Comment: C: Bamchop: Efficient Digest Of High-Throughput Sequencing Data In A Reproducible R
11.2 years ago by Ian 6.1k
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13k
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Answer: A: Convert Wiggle File From Hg18 To Hg19
11.2 years ago by Ian 6.1k
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6.7k
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Answer: A: Calculating Phastcons And Phylop Scores
11.2 years ago by Ian 6.1k
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4.4k
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Answer: A: A Question About Pair-End Reads Alignment
11.2 years ago by Ian 6.1k
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4.7k
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Answer: A: Rsat: How To Interpret Motif 'Sig' Scores In Peak-Motif?
11.3 years ago by Ian 6.1k
1
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4.7k
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Rsat: How To Interpret Motif 'Sig' Scores In Peak-Motif?
11.3 years ago by Ian 6.1k
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9.2k
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Comment: C: Generate Random Genomic Regions
11.3 years ago by Ian 6.1k
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9.2k
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Answer: A: Generate Random Genomic Regions
11.3 years ago by Ian 6.1k
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6.2k
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Answer: A: Download Older Versions Of Refseq?
11.3 years ago by Ian 6.1k
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0
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3.6k
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Answer: A: Phastcons Scores Instead Of Phylop Scores
11.3 years ago by Ian 6.1k
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4.2k
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Comment: C: Illumina'S New Reduced Resolution Q (Phred) Scores - Good Or Bad?
11.3 years ago by Ian 6.1k
17
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4
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4.2k
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Illumina'S New Reduced Resolution Q (Phred) Scores - Good Or Bad?
illumina
updated 11.3 years ago by 9.7k • written 11.3 years ago by 6.1k
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34k
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Comment: C: Fastq Quality Control Shootout
11.4 years ago by Ian 6.1k
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3.2k
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Answer: A: Rna-Seq : How To Check For Very High Coverage Region
11.4 years ago by Ian 6.1k
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2
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3.5k
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Answer: A: Chip-Seq For Mitochondrial Genes
11.4 years ago by Ian 6.1k
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4.1k
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Answer: A: How To Determine If Genomic Region Is Closer To A Centromere/Telomere
11.4 years ago by Ian 6.1k
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1
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2.5k
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Comment: C: Motif And Down Stream Analysis
11.4 years ago by Ian 6.1k
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1
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2.5k
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Comment: C: Motif And Down Stream Analysis
11.4 years ago by Ian 6.1k
1
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1
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3.4k
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Forum: Chip-Seq Analysis Using Galaxy
galaxy chip-seq
updated 21 months ago by 44k • written 11.4 years ago by 6.1k
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7.0k
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Comment: C: Sam Tools Pileup Format
11.5 years ago by Ian 6.1k
2
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1
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7.0k
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Answer: A: Sam Tools Pileup Format
11.5 years ago by Ian 6.1k
3
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40k
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Answer: A: Bedtools Genomecoveragebed Usage : How To Create A Genome File?
11.6 years ago by Ian 6.1k
1
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4.0k
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Answer: A: Tools For Quality Trimming Of Solid Reads In Colorspace.
11.6 years ago by Ian 6.1k
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0
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26k
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Comment: C: How Can I Generate A Venn Diagram In R For A Given Csv File
11.6 years ago by Ian 6.1k
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1
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2.7k
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Answer: A: What Are The Top 10 Ways That You Find Galaxy Most Useful For Whole Genome Seque
updated 11.6 years ago by 101k • written 11.6 years ago by 6.1k
5
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1
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3.5k
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Can Variants Be Reliably Detected In Duplicated Gene/Region Sequence?
variant-calling
updated 11.6 years ago by 28k • written 11.6 years ago by 6.1k
0
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8.2k
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Comment: C: Chip-Seq Peak Calling Using Macs In Galaxy- Overlapping Peaks For Replicates
11.6 years ago by Ian 6.1k
3
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0
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16k
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Answer: A: Is There Any Advantage Of Paired End Sequencing For Chip-Seq?
11.6 years ago by Ian 6.1k
0
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1
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9.5k
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Answer: A: Annotate Chip-Peaks With Gene Symbol/Name
11.6 years ago by Ian 6.1k
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1
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9.5k
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Comment: C: Annotate Chip-Peaks With Gene Symbol/Name
11.6 years ago by Ian 6.1k
1
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0
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2.9k
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Answer: A: Affyid Mapping Without Chip Info
11.7 years ago by Ian 6.1k
0
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0
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2.5k
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Answer: A: What Better Way To Get The Paired Reads Aligned Against The Reference Genome?
11.7 years ago by Ian 6.1k
0
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1
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3.3k
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Answer: A: Is It Acceptable To Merge Control Replicates When Doing Peak Detection In Faire-
11.7 years ago by Ian 6.1k
5
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0
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9.5k
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Answer: A: Why Are There Ambiguous (N) Bases (Gaps) In The Human Genome
11.7 years ago by Ian 6.1k
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0
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3.0k
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Comment: C: Is It Possible To Manually Reorder Steps In A Galaxy Workflow Summary?
11.7 years ago by Ian 6.1k
1
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7.8k
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Comment: C: Get A Graphical Representation Of Number Of Reads In Bam File For A Certain Geno
11.7 years ago by Ian 6.1k
1
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0
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4.3k
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Answer: A: What To Do About Negative Strand Coordinates In A Chip-Seq Peak Calling Analysis
11.7 years ago by Ian 6.1k
2
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0
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6.4k
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Answer: A: Get Conservation Score Of Chromosome Region
11.7 years ago by Ian 6.1k
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2
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4.9k
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Comment: C: How To Match Genes That Were Labeled Via Different Naming/Identification Standar
11.7 years ago by Ian 6.1k
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0
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7.7k
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Comment: C: P Value Or Statistical Significance Of Real Peak Compared To Random Peak Overlap
11.7 years ago by Ian 6.1k
1
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2
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4.9k
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Answer: A: How To Match Genes That Were Labeled Via Different Naming/Identification Standar
updated 3.7 years ago by 44k • written 11.7 years ago by 6.1k
467 results • Page 6 of 10
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