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Comment: Comment: Shallow sequencing is not a random subsample of deep sequencing
11 months ago by jockbanan ▴ 440
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2
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669
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Shallow sequencing is not a random subsample of deep sequencing
Illumina scRNA-seq
11 months ago by jockbanan ▴ 440
19
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8
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23k
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7 follow
rRNA Removal In Rna-Seq Data
rna-seq deseq
updated 2.5 years ago by • 0 • written 11.6 years ago by ▴ 440
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1
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5.3k
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Comment: Comment: Clustering of short peptide sequences
4.2 years ago by jockbanan ▴ 440
6
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3
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5.3k
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Tool: Clustering of short peptide sequences
peptide phage-display clustering
updated 2.8 years ago by 45k • written 9.7 years ago by ▴ 440
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0
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1.3k
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Answer: A: Pooling WT and CRISPR/Cas9 KOs cells in the same scRNAseq sample and then demult
4.6 years ago by jockbanan ▴ 440
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1
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3.0k
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Answer: A: CROP-seq data analysis
5.4 years ago by jockbanan ▴ 440
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0
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25k
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Answer: A: Data Visualisation -- Exon/Intron Map?
updated 5.7 years ago by 45k • written 11.9 years ago by ▴ 440
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1
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4.4k
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Comment: A: Where is the IGV hg38 gene track from
5.9 years ago by jockbanan ▴ 440
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0
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5.0k
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Comment: Comment: Trimmomatic does not trim custom adapters in palindrome mode
updated 2.5 years ago by 45k • written 10.0 years ago by ▴ 440
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1
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5.0k
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Comment: Comment: Trimmomatic does not trim custom adapters in palindrome mode
updated 2.5 years ago by 45k • written 10.0 years ago by ▴ 440
3
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5
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5.0k
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Trimmomatic does not trim custom adapters in palindrome mode
software-error next-gen trimmomatic
updated 2.5 years ago by 45k • written 10.0 years ago by ▴ 440
0
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0
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5.0k
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Answer: Answer: How to cluster (nearest neighbour method) amino acid peptide sequences based on
updated 3.2 years ago by 45k • written 10.4 years ago by ▴ 440
3
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0
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7.6k
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Answer: Answer: Visualizing Hmm Files Of Hmmer3
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 440
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1
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44k
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Comment: C: Pca From Vcf Files
updated 11.2 years ago by 4.2k • written 11.3 years ago by ▴ 440
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5.0k
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Comment: C: Multi-Sample Somatic Mutation Calling
11.3 years ago by jockbanan ▴ 440
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0
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5.0k
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Comment: C: Multi-Sample Somatic Mutation Calling
11.3 years ago by jockbanan ▴ 440
2
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8
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5.0k
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Multi-Sample Somatic Mutation Calling
snp variant-calling somatic mutation variant cancer
updated 11.3 years ago by 7.3k • written 11.3 years ago by ▴ 440
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1
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10.0k
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Answer: A: To What Degree Could We Determine Whether A Gene Is Expressed?
11.3 years ago by jockbanan ▴ 440
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4.6k
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Answer: A: Which Snp Caller / Method To Use After Aligning Rna-Seq With Tophat
11.3 years ago by jockbanan ▴ 440
3
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1
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10k
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Answer: A: How To Get The Kegg Pathway Name After Enrichment Analysis Using Kegg.Db From Bi
11.4 years ago by jockbanan ▴ 440
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1
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10k
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Comment: C: Rna-Seq: Treat Samples As Biological Replicates?
11.4 years ago by jockbanan ▴ 440
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0
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10k
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Comment: C: Rna-Seq: Treat Samples As Biological Replicates?
11.4 years ago by jockbanan ▴ 440
21
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10
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10k
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6 follow
Rna-Seq: Treat Samples As Biological Replicates?
rna-seq replicates
updated 11.4 years ago by ★ 2.2k • written 11.5 years ago by ▴ 440
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2
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23k
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Comment: C: Rrna Removal In Rna-Seq Data
11.6 years ago by jockbanan ▴ 440
0
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1
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1.9k
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Comment: C: Where Can I Find The Detailed Hhr-File Description? Hhsuite User Manual Has Not
11.6 years ago by jockbanan ▴ 440
9
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2
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17k
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Comment: C: Aligning Reads To A Reference Transcriptome
11.6 years ago by jockbanan ▴ 440
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0
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2.6k
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Answer: A: Computing The Number Of Possible Rna Secondary Structures
11.8 years ago by jockbanan ▴ 440
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0
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14k
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Answer: A: How To Perform A Blast Search From A Java Application?
11.8 years ago by jockbanan ▴ 440
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0
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7.2k
views
Answer: A: Help With Fisher Test For A More Than Two Group Of Genes‏
11.8 years ago by jockbanan ▴ 440
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