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Answer: A: Aligning transcript with known position for SNP to draft genome to find the posi
5.3 years ago by Vitis ★ 2.5k
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1.7k
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Answer: A: processing amplicon seq data from miseq
5.3 years ago by Vitis ★ 2.5k
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1.8k
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Answer: A: How to identify a species is autopolyploid or allopolyploid by high-throughput s
5.3 years ago by Vitis ★ 2.5k
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Answer: A: Mapping Gene Models Back to a Reference Genome of Closely Related Species
5.3 years ago by Vitis ★ 2.5k
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1.5k
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Answer: A: Making BAM or SAM files equivalent
5.4 years ago by Vitis ★ 2.5k
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3.7k
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Answer: A: How can I tell if there is CNV for specific gene in IGV?
5.4 years ago by Vitis ★ 2.5k
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1.1k
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Answer: A: Need help to separate a genome in different x coverage
5.5 years ago by Vitis ★ 2.5k
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2.1k
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Answer: A: Depth of Coverage without Read Overlap
5.5 years ago by Vitis ★ 2.5k
2
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5.0k
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Answer: A: Is there a tool or method for phasing a VCF based on an already phased BAM?
5.5 years ago by Vitis ★ 2.5k
2
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4.1k
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Answer: A: compare groups/populations - vcf files
5.5 years ago by Vitis ★ 2.5k
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2.4k
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Answer: A: How to extract coordinate of hard and soft clipped long reads ?
5.5 years ago by Vitis ★ 2.5k
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3.9k
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Answer: A: finding exons and introns sequences
5.5 years ago by Vitis ★ 2.5k
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1.7k
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Answer: A: Pulling out the reads associated with a vcf line entry.
5.5 years ago by Vitis ★ 2.5k
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2.3k
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Answer: A: How to create scatter plot with small pie charts?
5.5 years ago by Vitis ★ 2.5k
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7.2k
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Answer: A: Analysis gff3 file
5.5 years ago by Vitis ★ 2.5k
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7.2k
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Answer: A: Time-course RNA-seq analysis in Deseq2
5.5 years ago by Vitis ★ 2.5k
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1.6k
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Answer: A: Diploid sequences in ModelTest-NG: consensus or ambiguous sites?
5.5 years ago by Vitis ★ 2.5k
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5.6k
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Answer: A: [mpileup] 1 samples in 1 input files Is it an error?
5.6 years ago by Vitis ★ 2.5k
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4.2k
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Answer: A: GO enrichment analysis using R
6.2 years ago by Vitis ★ 2.5k
2
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2.9k
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Answer: A: How to run SnpEff for Tomato 2.5 (S_lycopersicum_chromosomes.2.50) reference, gf
7.3 years ago by Vitis ★ 2.5k
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5.5k
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Answer: A: splitting Multifasta File Into A *Smaller Multifasta File containing few sequenc
7.4 years ago by Vitis ★ 2.5k
0
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1
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1.6k
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Answer: A: comparing two tracks over intervals on the genome
7.4 years ago by Vitis ★ 2.5k
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2.5k
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Answer: A: How to grep ^I0.0^I in blast outfmt 6
7.4 years ago by Vitis ★ 2.5k
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6.9k
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Answer: A: Raw Read count from bam file
7.4 years ago by Vitis ★ 2.5k
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5.2k
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Answer: A: To extract unmapped pair end reads
7.4 years ago by Vitis ★ 2.5k
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7.7k
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Answer: A: vcf split by columns
7.4 years ago by Vitis ★ 2.5k
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3.6k
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Answer: A: RNAseq read depth
7.4 years ago by Vitis ★ 2.5k
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1.6k
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Answer: A: Genome-Wide Sequencing Depth of Coverage Relationship to Genomic Regional Variat
7.4 years ago by Vitis ★ 2.5k
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1.5k
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Answer: A: allele frequencies, genotype
7.4 years ago by Vitis ★ 2.5k
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7.0k
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Answer: A: Which Genome Synteny Program?
10.6 years ago by Vitis ★ 2.5k
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2.2k
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Answer: A: Snp Selection For Genotyping
10.7 years ago by Vitis ★ 2.5k
2
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4.6k
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Answer: A: Online Interactive Data Visualization
10.7 years ago by Vitis ★ 2.5k
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0
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4.3k
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Answer: A: Read Counts From Sam File Mapped To De Novo Assembled Transcripts Using Htseq-Co
10.7 years ago by Vitis ★ 2.5k
2
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1
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4.5k
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Answer: A: What Do You Expect As The False Positive And Negative Rate For Snp'S And Indels
10.8 years ago by Vitis ★ 2.5k
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2.1k
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Answer: A: How To Exon-Intron Map With Given Coordinates?
10.8 years ago by Vitis ★ 2.5k
3
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1
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4.3k
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Answer: A: Looking For A Good Open Source Command-Line Sanger Sequence Pairwise Assembler
10.8 years ago by Vitis ★ 2.5k
1
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0
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3.4k
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Answer: A: Snps To Protein Domain
10.9 years ago by Vitis ★ 2.5k
1
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0
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7.7k
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Answer: A: Is There A Query Parameter For The Online Blast That Would Filter For Hits That
11.0 years ago by Vitis ★ 2.5k
0
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0
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40k
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Answer: A: Plotting Density Of Snps On Chromosomes
11.2 years ago by Vitis ★ 2.5k
1
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0
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8.5k
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Answer: A: Best Tools For Motif Finding And/Or De Novo Motif Discovery?
11.8 years ago by Vitis ★ 2.5k
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0
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4.7k
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Answer: A: Program To Align Cdna And Dna Genomic
11.8 years ago by Vitis ★ 2.5k
1
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1
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2.8k
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Answer: A: Phylogenetic Analysis Of Gene Enrichment?
11.9 years ago by Vitis ★ 2.5k
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0
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7.3k
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Answer: A: Building A Webpage For Accessing Rna-Seq Expression Data
12.0 years ago by Vitis ★ 2.5k
1
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0
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6.4k
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Answer: A: De Novo Transcriptome And Comparative Genomics
12.0 years ago by Vitis ★ 2.5k
6
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6
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15k
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Answer: A: Rna-Seq Data Variant Calling
12.1 years ago by Vitis ★ 2.5k
1
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0
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2.4k
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Answer: A: The Methods To Determine Mads-Box Gene Families In A Newly Sequenced Genome? I N
12.1 years ago by Vitis ★ 2.5k
1
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0
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6.4k
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Answer: A: Is It Necessary To Do Read Trimming For Rna-Seq Data?
12.1 years ago by Vitis ★ 2.5k
0
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0
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15k
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Answer: A: Hierarchical Clustering-Dendrogram Cut-Off
12.1 years ago by Vitis ★ 2.5k
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4.5k
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Answer: A: Problems With Orthomclblastparser Script
12.2 years ago by Vitis ★ 2.5k
0
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0
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2.4k
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Answer: A: How To Display Reads Profiling By Sense And Antise Separately Using Gbrowse?
12.2 years ago by Vitis ★ 2.5k
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