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Comment: C: What Would You Do With Your Personal Genome Data?
updated 3.7 years ago by 39k • written 11.8 years ago by ▴ 620
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4.0k
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Answer: A: Batch Search Effect Of A Snp On Protein (Conserved) Domain
updated 3.8 years ago by 39k • written 12.4 years ago by ▴ 620
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Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, Mugs, Etc
updated 5.4 years ago by • 0 • written 11.1 years ago by ▴ 620
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Comment: C: Method To Identify Viral Integration Site In Human Genome From Ngs Data?
5.6 years ago by Bioinfosm ▴ 620
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Comment: C: RNA-SeQC, EVER-seq, RSeQC and CollectRnaSeqMetrics, which to use and *why*?
8.0 years ago by Bioinfosm ▴ 620
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Comment: Comment: Plot Coverage Vs. Gc Content
updated 5 months ago by 39k • written 8.0 years ago by ▴ 620
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Comment: C: Do read pairs matter in alignment?
8.2 years ago by Bioinfosm ▴ 620
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2.8k
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Answer: A: Do read pairs matter in alignment?
8.2 years ago by Bioinfosm ▴ 620
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Comment: C: Amino Acid Change To Genomic Location
9.7 years ago by Bioinfosm ▴ 620
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27k
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Comment: C: Amino Acid Change To Genomic Location
9.7 years ago by Bioinfosm ▴ 620
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1
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27k
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Comment: C: Amino Acid Change To Genomic Location
9.7 years ago by Bioinfosm ▴ 620
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7 follow
Resources For Video/Webcasts Of Talks/Seminars/Courses
updated 14 months ago by 39k • written 11.1 years ago by ▴ 620
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6.5k
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Comment: C: Get A Graphical Representation Of Number Of Reads In Bam File For A Certain Geno
10.2 years ago by Bioinfosm ▴ 620
42
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21
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40k
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11 follow
Comparing 2 Large Lists (Millions Of Rows) To Identify Shared And Exclusive Elements
unix list intersect
updated 18 months ago by 39k • written 10.3 years ago by ▴ 620
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Comment: C: Does It Makes Sense To Assemble All My Rna-Seq Samples As Though They Were One?
10.2 years ago by Bioinfosm ▴ 620
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Comment: C: Resources For Video/Webcasts Of Talks/Seminars/Courses
10.6 years ago by Bioinfosm ▴ 620
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3.0k
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Answer: A: Identification Of Relevant Germline Mutations In Illumina Data.... Filtering Str
11.0 years ago by Bioinfosm ▴ 620
12
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5
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8.4k
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How To Quantify Unmapped Reads
next-gen sequencing
updated 11.0 years ago by 13k • written 11.0 years ago by ▴ 620
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8.4k
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Comment: C: How To Quantify Unmapped Reads
11.0 years ago by Bioinfosm ▴ 620
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Comment: C: Chipseq Data On Prostate Cancer
11.0 years ago by Bioinfosm ▴ 620
5
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3
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2.8k
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Chipseq Data On Prostate Cancer
chip-seq cancer next-gen
updated 9 months ago by 39k • written 11.0 years ago by ▴ 620
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5.4k
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Comment: C: Extracting The Base/Nucleotide Across All Reads At Particular Position/S.
11.1 years ago by Bioinfosm ▴ 620
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1
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2.5k
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What Are Some Of The Useful Genomics/Bioinformatics Apps For Phone/Ipad?
updated 11.1 years ago by ★ 3.1k • written 11.1 years ago by ▴ 620
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Comment: C: R -- Get Exonic Ranges Of A Gene'S Transcripts Given Its Name?
11.1 years ago by Bioinfosm ▴ 620
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1
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15k
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Answer: A: I Am Preparing A Course On Ngs: Any Suggestion ?
11.1 years ago by Bioinfosm ▴ 620
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Comment: C: Plos Paper - Rise And Demise Of Bioinformatics... Overly Negative Undertones
11.1 years ago by Bioinfosm ▴ 620
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8
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2.1k
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Forum: Plos Paper - Rise And Demise Of Bioinformatics... Overly Negative Undertones
bioinformatics
updated 3 months ago by 39k • written 11.1 years ago by ▴ 620
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3.0k
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Comment: C: Tophat Gene Models Merging
11.1 years ago by Bioinfosm ▴ 620
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3
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3.0k
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Tophat Gene Models Merging
tophat rna-seq
updated 11.1 years ago by ★ 1.2k • written 11.1 years ago by ▴ 620
3
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1
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26k
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Answer: A: Why You Need Perl/Python If You Know R/Shell [Ngs Data Analysis]
updated 11.1 years ago by 12k • written 11.1 years ago by ▴ 620
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Comment: C: Resources For Video/Webcasts Of Talks/Seminars/Courses
11.1 years ago by Bioinfosm ▴ 620
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1
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2.6k
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Comment: C: Calling Genotypes On Multiple Trios
11.1 years ago by Bioinfosm ▴ 620
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3.2k
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Comment: C: Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, M
11.1 years ago by Bioinfosm ▴ 620
3
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2
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2.6k
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Answer: A: Calling Genotypes On Multiple Trios
11.1 years ago by Bioinfosm ▴ 620
0
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1
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3.2k
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Comment: C: Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, M
11.1 years ago by Bioinfosm ▴ 620
1
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0
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3.2k
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Comment: C: Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, M
11.1 years ago by Bioinfosm ▴ 620
0
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2.6k
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Answer: A: Retrieve One Coding Sequences For Each Gene
11.1 years ago by Bioinfosm ▴ 620
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41k
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Comment: C: Why Are There Many Rna-Seq Hits To Intronic Regions?
11.1 years ago by Bioinfosm ▴ 620
2
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1
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4.2k
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Answer: A: Where To Find A Good Estimate Of The Background Mutation Rate In Rattus Norvegic
11.2 years ago by Bioinfosm ▴ 620
1
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1
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3.1k
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Answer: A: Does It Makes Sense To Assemble All My Rna-Seq Samples As Though They Were One?
11.2 years ago by Bioinfosm ▴ 620
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0
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2.5k
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Answer: A: Snp Positions Along A Read
11.2 years ago by Bioinfosm ▴ 620
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4.9k
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Answer: A: Quality Analysis Of Pacbio Data
11.2 years ago by Bioinfosm ▴ 620
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1
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14k
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Comment: C: Rna-Seq Data Variant Calling
11.2 years ago by Bioinfosm ▴ 620
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9.9k
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Comment: C: Genomic Positions Of Protein Domains
11.3 years ago by Bioinfosm ▴ 620
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4.8k
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Comment: C: How To Check If The Iupac Snp Code Changes Translation ?
11.3 years ago by Bioinfosm ▴ 620
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0
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2.2k
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Comment: C: Sliderii For Deep Coverage
11.6 years ago by Bioinfosm ▴ 620
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5.0k
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Comment: C: Can We Agree On A Short Twitter Hashtag For Nextgen Sequencing?
11.6 years ago by Bioinfosm ▴ 620
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5.0k
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Comment: C: Aminoacid Composition Using Biopython
11.8 years ago by Bioinfosm ▴ 620
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4
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6.3k
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Answer: A: What Would You Do With Your Personal Genome Data?
11.8 years ago by Bioinfosm ▴ 620
1
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0
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3.8k
views
Answer: A: How To Predict Which Next Gen Variants Would Not Validate By Sanger
11.8 years ago by Bioinfosm ▴ 620
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