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5
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2
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3.6k
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Answer: A: Machine learning procedure for cancer subtype discovery
10.4 years ago by Mikael Huss 4.8k
0
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0
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3.5k
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Comment: C: What Could Be The Reason For Spliced Alignments In Chip-Seq Data?
10.4 years ago by Mikael Huss 4.8k
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0
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22k
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Comment: C: Which software do you use for RNA-seq data quality control?
10.5 years ago by Mikael Huss 4.8k
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1
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3.7k
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Comment: C: RNA-Seq: can one implicate viruses if unmapped reads map to virus sequences?
10.5 years ago by Mikael Huss 4.8k
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1
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3.7k
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Comment: C: RNA-Seq: can one implicate viruses if unmapped reads map to virus sequences?
10.5 years ago by Mikael Huss 4.8k
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0
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4.8k
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Comment: C: Why does trinity and cufflink use bowtie to align reads back to assembled reads?
10.5 years ago by Mikael Huss 4.8k
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0
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3.5k
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Comment: C: What Could Be The Reason For Spliced Alignments In Chip-Seq Data?
10.5 years ago by Mikael Huss 4.8k
4
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0
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2.6k
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Answer: A: Chip-Seq Of Conventional Tfs: What Are The Peaks W/O The Motif?
10.6 years ago by Mikael Huss 4.8k
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1
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13k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.6 years ago by Mikael Huss 4.8k
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0
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13k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.6 years ago by Mikael Huss 4.8k
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0
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13k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.6 years ago by Mikael Huss 4.8k
0
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0
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13k
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Comment: C: Best Way To Quantify Influence Of Different Covariates On Gene Expression?
10.6 years ago by Mikael Huss 4.8k
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0
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4.2k
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Comment: C: Cufflinks Skips Loci, Marks With Hidata
10.7 years ago by Mikael Huss 4.8k
2
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0
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2.4k
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Answer: A: What Can We Do For The Reads That Are Not Mapped To The Genome?
10.7 years ago by Mikael Huss 4.8k
0
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1
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4.2k
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Comment: C: Cufflinks Skips Loci, Marks With Hidata
10.7 years ago by Mikael Huss 4.8k
0
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1
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4.2k
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Answer: A: Cufflinks Skips Loci, Marks With Hidata
10.7 years ago by Mikael Huss 4.8k
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0
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4.2k
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Comment: C: Where To Find Encode Dnase I Footprint Data
10.7 years ago by Mikael Huss 4.8k
2
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0
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4.7k
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Answer: Answer: Publicly Available Rna-Seq Data For Study Splicing Change In Human Brain
updated 3.6 years ago by 44k • written 10.8 years ago by 4.8k
1
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0
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2.0k
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Answer: A: Bioinformatics And Graph Platforms Like "Powergraph" Or "Graphlab"
10.8 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: How To Improve Whole Genome Assembly Quality
10.8 years ago by Mikael Huss 4.8k
1
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0
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107k
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Comment: C: How To Calculate Fpkm (Fragments Per Kilobase Of Exon Per Million Fragments Mapp
10.8 years ago by Mikael Huss 4.8k
1
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0
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3.6k
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Comment: C: What Are The Main Advantages Of Ngs Over Arrays In Transcriptomics?
10.8 years ago by Mikael Huss 4.8k
4
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1
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4.3k
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Answer: A: What Will Happen If One Read Can Map To Two Regions?
10.9 years ago by Mikael Huss 4.8k
6
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0
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18k
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Answer: A: How Can We Get Tissue Specific Genes?
10.9 years ago by Mikael Huss 4.8k
0
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0
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9.6k
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Comment: C: Rna-Seq: Treat Samples As Biological Replicates?
10.9 years ago by Mikael Huss 4.8k
4
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1
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9.6k
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Answer: A: Rna-Seq: Treat Samples As Biological Replicates?
10.9 years ago by Mikael Huss 4.8k
0
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0
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4.1k
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Comment: C: Determining Most Diagnostic Differentially Expressed Genes
11.0 years ago by Mikael Huss 4.8k
0
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1
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2.9k
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Answer: A: Macs Chip-Seq Contorl
11.0 years ago by Mikael Huss 4.8k
1
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0
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3.6k
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Comment: C: Fast Rna-Seq Exon Count Calculation
11.1 years ago by Mikael Huss 4.8k
1
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2
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3.6k
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Comment: C: Fast Rna-Seq Exon Count Calculation
11.1 years ago by Mikael Huss 4.8k
2
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0
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4.9k
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Comment: C: Does Anyone Know If One Can Access The Seqc Data
11.1 years ago by Mikael Huss 4.8k
0
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0
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4.9k
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Comment: C: Does Anyone Know If One Can Access The Seqc Data
11.1 years ago by Mikael Huss 4.8k
0
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1
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4.9k
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Comment: C: Does Anyone Know If One Can Access The Seqc Data
11.1 years ago by Mikael Huss 4.8k
2
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1
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4.9k
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Answer: A: Does Anyone Know If One Can Access The Seqc Data
11.1 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
11.1 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.
11.1 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.
11.1 years ago by Mikael Huss 4.8k
2
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0
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4.7k
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Answer: A: Is It Okay To Remove Chrun And Chr*_Random Reads From A Bed File?
11.1 years ago by Mikael Huss 4.8k
0
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0
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8.9k
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Comment: C: Tools For Analysis Allele Specific Expression In Rna-Seq Data?
11.1 years ago by Mikael Huss 4.8k
0
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0
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2.4k
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Comment: C: Some Software That Can Assemble The Dna Sequence From Ngs Even If It Is From Mix
11.1 years ago by Mikael Huss 4.8k
1
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1
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8.9k
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Answer: A: Tools For Analysis Allele Specific Expression In Rna-Seq Data?
11.1 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
11.1 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
11.1 years ago by Mikael Huss 4.8k
3
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1
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7.6k
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Answer: A: Rna Seq: Alignment Pipeline Using Tophat - Opinion Pls!
11.2 years ago by Mikael Huss 4.8k
2
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1
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2.4k
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Answer: A: Some Software That Can Assemble The Dna Sequence From Ngs Even If It Is From Mix
11.2 years ago by Mikael Huss 4.8k
1
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1
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6.3k
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Comment: C: Is It A Good Idea To Trim Rna-Seq Reads Or Just Remove N'S?
11.2 years ago by Mikael Huss 4.8k
0
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0
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9.4k
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Comment: C: The Five Most Annoying Bioinformatics Problems You Face Every Week?
11.2 years ago by Mikael Huss 4.8k
3
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1
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6.3k
views
Answer: A: Is It A Good Idea To Trim Rna-Seq Reads Or Just Remove N'S?
11.2 years ago by Mikael Huss 4.8k
0
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1
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9.4k
views
Answer: A: The Five Most Annoying Bioinformatics Problems You Face Every Week?
11.2 years ago by Mikael Huss 4.8k
0
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0
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14k
views
Comment: C: Ncbi Refseq Viral Genomes
11.2 years ago by Mikael Huss 4.8k
293 results • Page 2 of 6
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