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Comment: C: What Would You Do With Your Personal Genome Data?
updated 5.7 years ago by 45k • written 13.8 years ago by ▴ 620
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5.1k
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Answer: A: Batch Search Effect Of A Snp On Protein (Conserved) Domain
updated 5.8 years ago by 45k • written 14.4 years ago by ▴ 620
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Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, Mugs, Etc
updated 7.4 years ago by • 0 • written 13.2 years ago by ▴ 620
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Comment: C: Method To Identify Viral Integration Site In Human Genome From Ngs Data?
7.6 years ago by Bioinfosm ▴ 620
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Comment: C: RNA-SeQC, EVER-seq, RSeQC and CollectRnaSeqMetrics, which to use and *why*?
10.0 years ago by Bioinfosm ▴ 620
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Comment: Comment: Plot Coverage Vs. Gc Content
updated 2.5 years ago by 45k • written 10.0 years ago by ▴ 620
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Comment: C: Do read pairs matter in alignment?
10.2 years ago by Bioinfosm ▴ 620
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3.5k
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Answer: A: Do read pairs matter in alignment?
10.3 years ago by Bioinfosm ▴ 620
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33k
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Comment: C: Amino Acid Change To Genomic Location
11.8 years ago by Bioinfosm ▴ 620
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33k
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Comment: C: Amino Acid Change To Genomic Location
11.8 years ago by Bioinfosm ▴ 620
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1
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33k
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Comment: C: Amino Acid Change To Genomic Location
11.8 years ago by Bioinfosm ▴ 620
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7 follow
Resources For Video/Webcasts Of Talks/Seminars/Courses
updated 3.2 years ago by 45k • written 13.2 years ago by ▴ 620
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1
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8.8k
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Comment: C: Get A Graphical Representation Of Number Of Reads In Bam File For A Certain Geno
12.3 years ago by Bioinfosm ▴ 620
42
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21
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45k
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11 follow
Comparing 2 Large Lists (Millions Of Rows) To Identify Shared And Exclusive Elements
unix list intersect
updated 3.6 years ago by 45k • written 12.4 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?
12.3 years ago by Bioinfosm ▴ 620
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Comment: C: Resources For Video/Webcasts Of Talks/Seminars/Courses
12.7 years ago by Bioinfosm ▴ 620
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3.6k
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Answer: A: Identification Of Relevant Germline Mutations In Illumina Data.... Filtering Str
13.0 years ago by Bioinfosm ▴ 620
12
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5
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10.0k
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How To Quantify Unmapped Reads
next-gen sequencing
updated 13.1 years ago by 15k • written 13.1 years ago by ▴ 620
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10.0k
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Comment: C: How To Quantify Unmapped Reads
13.1 years ago by Bioinfosm ▴ 620
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Comment: C: Chipseq Data On Prostate Cancer
13.1 years ago by Bioinfosm ▴ 620
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3
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3.3k
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Chipseq Data On Prostate Cancer
chip-seq cancer next-gen
updated 2.8 years ago by 45k • written 13.1 years ago by ▴ 620
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1
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6.4k
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Comment: C: Extracting The Base/Nucleotide Across All Reads At Particular Position/S.
13.1 years ago by Bioinfosm ▴ 620
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1
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2.9k
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What Are Some Of The Useful Genomics/Bioinformatics Apps For Phone/Ipad?
updated 13.1 years ago by ★ 3.2k • written 13.1 years ago by ▴ 620
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Comment: C: R -- Get Exonic Ranges Of A Gene'S Transcripts Given Its Name?
13.1 years ago by Bioinfosm ▴ 620
4
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1
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19k
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Answer: A: I Am Preparing A Course On Ngs: Any Suggestion ?
13.1 years ago by Bioinfosm ▴ 620
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3.1k
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Comment: C: Plos Paper - Rise And Demise Of Bioinformatics... Overly Negative Undertones
13.1 years ago by Bioinfosm ▴ 620
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8
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3.1k
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Forum: Plos Paper - Rise And Demise Of Bioinformatics... Overly Negative Undertones
bioinformatics
updated 2.3 years ago by 45k • written 13.1 years ago by ▴ 620
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3.5k
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Comment: C: Tophat Gene Models Merging
13.1 years ago by Bioinfosm ▴ 620
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3
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3.5k
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Tophat Gene Models Merging
tophat rna-seq
updated 13.1 years ago by ★ 1.2k • written 13.1 years ago by ▴ 620
3
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1
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29k
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Answer: A: Why You Need Perl/Python If You Know R/Shell [Ngs Data Analysis]
updated 13.2 years ago by 12k • written 13.2 years ago by ▴ 620
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2
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Comment: C: Resources For Video/Webcasts Of Talks/Seminars/Courses
13.2 years ago by Bioinfosm ▴ 620
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1
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3.6k
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Comment: C: Calling Genotypes On Multiple Trios
13.2 years ago by Bioinfosm ▴ 620
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4.2k
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Comment: C: Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, M
13.2 years ago by Bioinfosm ▴ 620
3
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2
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3.6k
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Answer: A: Calling Genotypes On Multiple Trios
13.2 years ago by Bioinfosm ▴ 620
0
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1
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4.2k
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Comment: C: Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, M
13.2 years ago by Bioinfosm ▴ 620
1
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0
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4.2k
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Comment: C: Recommendations For Good Bioinformatics Memorabilia And 'Stuff' Like T-Shirts, M
13.2 years ago by Bioinfosm ▴ 620
0
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0
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3.1k
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Answer: A: Retrieve One Coding Sequences For Each Gene
13.2 years ago by Bioinfosm ▴ 620
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0
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51k
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Comment: C: Why Are There Many Rna-Seq Hits To Intronic Regions?
13.2 years ago by Bioinfosm ▴ 620
2
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1
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4.7k
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Answer: A: Where To Find A Good Estimate Of The Background Mutation Rate In Rattus Norvegic
13.2 years ago by Bioinfosm ▴ 620
1
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1
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3.7k
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Answer: A: Does It Makes Sense To Assemble All My Rna-Seq Samples As Though They Were One?
13.2 years ago by Bioinfosm ▴ 620
0
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0
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2.8k
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Answer: A: Snp Positions Along A Read
13.2 years ago by Bioinfosm ▴ 620
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5.7k
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Answer: A: Quality Analysis Of Pacbio Data
13.2 years ago by Bioinfosm ▴ 620
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1
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16k
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Comment: C: Rna-Seq Data Variant Calling
13.2 years ago by Bioinfosm ▴ 620
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0
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12k
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Comment: C: Genomic Positions Of Protein Domains
13.4 years ago by Bioinfosm ▴ 620
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5.8k
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Comment: C: How To Check If The Iupac Snp Code Changes Translation ?
13.4 years ago by Bioinfosm ▴ 620
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0
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2.7k
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Comment: C: Sliderii For Deep Coverage
13.6 years ago by Bioinfosm ▴ 620
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8.8k
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Comment: C: Can We Agree On A Short Twitter Hashtag For Nextgen Sequencing?
13.6 years ago by Bioinfosm ▴ 620
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6.2k
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Comment: C: Aminoacid Composition Using Biopython
13.8 years ago by Bioinfosm ▴ 620
4
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4
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8.4k
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Answer: A: What Would You Do With Your Personal Genome Data?
13.8 years ago by Bioinfosm ▴ 620
1
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0
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5.1k
views
Answer: A: How To Predict Which Next Gen Variants Would Not Validate By Sanger
13.9 years ago by Bioinfosm ▴ 620
54 results • Page 1 of 2
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