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5
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2
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3.4k
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Answer: A: Machine learning procedure for cancer subtype discovery
9.8 years ago by Mikael Huss 4.8k
0
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0
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3.3k
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Comment: C: What Could Be The Reason For Spliced Alignments In Chip-Seq Data?
9.8 years ago by Mikael Huss 4.8k
1
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0
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21k
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Comment: C: Which software do you use for RNA-seq data quality control?
9.9 years ago by Mikael Huss 4.8k
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1
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3.5k
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Comment: C: RNA-Seq: can one implicate viruses if unmapped reads map to virus sequences?
9.9 years ago by Mikael Huss 4.8k
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1
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3.5k
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Comment: C: RNA-Seq: can one implicate viruses if unmapped reads map to virus sequences?
9.9 years ago by Mikael Huss 4.8k
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0
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4.6k
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Comment: C: Why does trinity and cufflink use bowtie to align reads back to assembled reads?
9.9 years ago by Mikael Huss 4.8k
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0
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3.3k
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Comment: C: What Could Be The Reason For Spliced Alignments In Chip-Seq Data?
9.9 years ago by Mikael Huss 4.8k
4
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0
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2.5k
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Answer: A: Chip-Seq Of Conventional Tfs: What Are The Peaks W/O The Motif?
10.0 years ago by Mikael Huss 4.8k
0
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1
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12k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.0 years ago by Mikael Huss 4.8k
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0
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12k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.0 years ago by Mikael Huss 4.8k
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0
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12k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.0 years ago by Mikael Huss 4.8k
0
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0
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12k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.0 years ago by Mikael Huss 4.8k
0
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0
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3.9k
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Comment: C: Cufflinks Skips Loci, Marks With Hidata
10.1 years ago by Mikael Huss 4.8k
2
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0
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2.2k
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Answer: A: What Can We Do For The Reads That Are Not Mapped To The Genome?
10.1 years ago by Mikael Huss 4.8k
0
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1
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3.9k
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Comment: C: Cufflinks Skips Loci, Marks With Hidata
10.1 years ago by Mikael Huss 4.8k
0
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1
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3.9k
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Answer: A: Cufflinks Skips Loci, Marks With Hidata
10.1 years ago by Mikael Huss 4.8k
0
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0
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4.0k
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Comment: C: Where To Find Encode Dnase I Footprint Data
10.2 years ago by Mikael Huss 4.8k
2
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0
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4.6k
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Answer: Answer: Publicly Available Rna-Seq Data For Study Splicing Change In Human Brain
updated 3.0 years ago by 43k • written 10.2 years ago by 4.8k
1
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0
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1.9k
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Answer: A: Bioinformatics And Graph Platforms Like "Powergraph" Or "Graphlab"
10.2 years ago by Mikael Huss 4.8k
0
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0
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8.1k
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Comment: C: How To Improve Whole Genome Assembly Quality
10.2 years ago by Mikael Huss 4.8k
1
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0
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106k
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Comment: C: How To Calculate Fpkm (Fragments Per Kilobase Of Exon Per Million Fragments Mapp
10.2 years ago by Mikael Huss 4.8k
1
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0
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3.5k
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Comment: C: What Are The Main Advantages Of Ngs Over Arrays In Transcriptomics?
10.2 years ago by Mikael Huss 4.8k
4
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1
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4.1k
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Answer: A: What Will Happen If One Read Can Map To Two Regions?
10.3 years ago by Mikael Huss 4.8k
6
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0
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17k
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Answer: A: How Can We Get Tissue Specific Genes?
10.3 years ago by Mikael Huss 4.8k
0
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0
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9.2k
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Comment: C: Rna-Seq: Treat Samples As Biological Replicates?
10.3 years ago by Mikael Huss 4.8k
4
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1
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9.2k
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Answer: A: Rna-Seq: Treat Samples As Biological Replicates?
10.3 years ago by Mikael Huss 4.8k
0
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0
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3.9k
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Comment: C: Determining Most Diagnostic Differentially Expressed Genes
10.4 years ago by Mikael Huss 4.8k
0
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1
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2.7k
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Answer: A: Macs Chip-Seq Contorl
10.4 years ago by Mikael Huss 4.8k
1
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0
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3.4k
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Comment: C: Fast Rna-Seq Exon Count Calculation
10.5 years ago by Mikael Huss 4.8k
1
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2
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3.4k
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Comment: C: Fast Rna-Seq Exon Count Calculation
10.5 years ago by Mikael Huss 4.8k
2
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0
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4.6k
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Comment: C: Does Anyone Know If One Can Access The Seqc Data
10.5 years ago by Mikael Huss 4.8k
0
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0
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4.6k
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Comment: C: Does Anyone Know If One Can Access The Seqc Data
10.5 years ago by Mikael Huss 4.8k
0
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1
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4.6k
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Comment: C: Does Anyone Know If One Can Access The Seqc Data
10.5 years ago by Mikael Huss 4.8k
2
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1
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4.6k
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Answer: A: Does Anyone Know If One Can Access The Seqc Data
10.5 years ago by Mikael Huss 4.8k
0
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1
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2.8k
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Answer: A: How To Tell How Many Reads Aligned To Intron In Tophat2
10.5 years ago by Mikael Huss 4.8k
0
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0
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19k
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Comment: C: Software To Find Overlaps Of Chip-Seq Peaks In Multiple Samples.
10.5 years ago by Mikael Huss 4.8k
0
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1
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19k
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Comment: C: Software To Find Overlaps Of Chip-Seq Peaks In Multiple Samples.
10.5 years ago by Mikael Huss 4.8k
2
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0
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4.4k
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Answer: A: Is It Okay To Remove Chrun And Chr*_Random Reads From A Bed File?
10.5 years ago by Mikael Huss 4.8k
0
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0
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8.7k
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Comment: C: Tools For Analysis Allele Specific Expression In Rna-Seq Data?
10.5 years ago by Mikael Huss 4.8k
0
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0
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2.3k
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Comment: C: Some Software That Can Assemble The Dna Sequence From Ngs Even If It Is From Mix
10.5 years ago by Mikael Huss 4.8k
1
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1
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8.7k
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Answer: A: Tools For Analysis Allele Specific Expression In Rna-Seq Data?
10.5 years ago by Mikael Huss 4.8k
0
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0
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11k
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Comment: C: Minimum Or Optimal Rpkm Value To Find If A Transcript Is Significant
10.5 years ago by Mikael Huss 4.8k
1
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1
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11k
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Comment: C: Minimum Or Optimal Rpkm Value To Find If A Transcript Is Significant
10.5 years ago by Mikael Huss 4.8k
3
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1
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7.4k
views
Answer: A: Rna Seq: Alignment Pipeline Using Tophat - Opinion Pls!
10.6 years ago by Mikael Huss 4.8k
2
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1
reply
2.3k
views
Answer: A: Some Software That Can Assemble The Dna Sequence From Ngs Even If It Is From Mix
10.6 years ago by Mikael Huss 4.8k
1
vote
1
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6.1k
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Comment: C: Is It A Good Idea To Trim Rna-Seq Reads Or Just Remove N'S?
10.6 years ago by Mikael Huss 4.8k
0
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0
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9.0k
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Comment: C: The Five Most Annoying Bioinformatics Problems You Face Every Week?
10.6 years ago by Mikael Huss 4.8k
3
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1
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6.1k
views
Answer: A: Is It A Good Idea To Trim Rna-Seq Reads Or Just Remove N'S?
10.6 years ago by Mikael Huss 4.8k
0
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1
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9.0k
views
Answer: A: The Five Most Annoying Bioinformatics Problems You Face Every Week?
10.6 years ago by Mikael Huss 4.8k
0
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0
replies
14k
views
Comment: C: Ncbi Refseq Viral Genomes
10.6 years ago by Mikael Huss 4.8k
293 results • Page 2 of 6
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