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Comment: C: Comparing contigs results from two different assembler
updated 4.3 years ago by 43k • written 8.2 years ago by 13k
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0
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2.6k
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Comment: C: PatternCNV : tool detects DNA copy number of variations
updated 4.3 years ago by 43k • written 9.9 years ago by 13k
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1
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3.2k
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Comment: C: CNV analysis from a family of 4 exome sequences
updated 4.3 years ago by 43k • written 9.9 years ago by 13k
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4.9k
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Comment: C: tophat Preparing reads [FAILED]
updated 4.3 years ago by 43k • written 9.9 years ago by 13k
1
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1
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3.2k
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Comment: C: CNV analysis from a family of 4 exome sequences
updated 4.3 years ago by 43k • written 9.9 years ago by 13k
0
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1
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3.2k
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Comment: C: Empty SomaticSniper Output Files
updated 4.3 years ago by 43k • written 9.9 years ago by 13k
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1.1k
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Comment: C: Homozygot genotype information but SNP is heterozygous
4.4 years ago by User 59 13k
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0
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3.2k
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Comment: C: MISO installation not creating settings file
updated 4.4 years ago by 43k • written 8.3 years ago by 13k
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2.3k
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Comment: C: Coverage depth and breadth after recaliberation
updated 4.4 years ago by 43k • written 8.3 years ago by 13k
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1
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4.8k
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Comment: C: Fusion gene detection software
updated 4.4 years ago by 43k • written 8.3 years ago by 13k
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0
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14k
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Comment: C: meaning of the Per tile sequence quality
updated 4.4 years ago by 43k • written 8.3 years ago by 13k
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1.8k
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Comment: C: Question about Ben Busby lecture #3 on NCBI now
updated 4.4 years ago by 43k • written 8.5 years ago by 13k
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0
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4.6k
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Comment: C: Should I use Illumina or Ion Torrent for producing data intended for genome rese
updated 4.4 years ago by 43k • written 8.5 years ago by 13k
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1
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13k
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Comment: C: Comparison Of Soap And Bwa
updated 4.6 years ago by 43k • written 12.1 years ago by 13k
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6.6k
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Comment: C: Masslynx Raw Directory Data Structure
updated 4.6 years ago by 43k • written 12.3 years ago by 13k
1
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4.9k
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Comment: C: Should We Release Database Dumps Of All Questions On Biostar?
updated 4.6 years ago by 43k • written 13.4 years ago by 13k
2
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6.5k
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Comment: C: Remove Known Snps From A Vcf File
updated 4.6 years ago by 43k • written 12.1 years ago by 13k
1
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0
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5.3k
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Comment: C: How About Starting A Tutorial For Chip Seq Data Analysis?
updated 4.6 years ago by 43k • written 12.9 years ago by 13k
1
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0
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5.5k
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Comment: C: Getting The Atom And Strands From A Pdb Xml File
updated 4.6 years ago by 43k • written 13.4 years ago by 13k
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0
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13k
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Comment: C: Combining Gene Expression Microarray Datasets
updated 4.6 years ago by 43k • written 13.4 years ago by 13k
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0
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2.6k
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Comment: C: Must I Have The .Sff Files In Order To Run Mira3
updated 4.7 years ago by 43k • written 13.7 years ago by 13k
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1
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2.1k
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Comment: C: defining function of list of genes
updated 5.6 years ago by 43k • written 8.2 years ago by 13k
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5.0k
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Comment: C: Indel Detection For 454 Resequencing
updated 5.6 years ago by 43k • written 13.5 years ago by 13k
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0
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2.1k
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Comment: C: Bioinformatician/Statistical Geneticist at Cytox Ltd (UK)
6.7 years ago by User 59 13k
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3.7k
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Comment: C: Somatic Mutation Identification without Paired Normal Sample
7.4 years ago by User 59 13k
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0
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3.4k
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Comment: C: How to differentiate between prokaryotic and eukaryotic transcript from RNAseq d
7.4 years ago by User 59 13k
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0
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8.0k
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Comment: C: Why we need 100X coverage to get a high-quality assembly?
7.4 years ago by User 59 13k
2
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1
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2.0k
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Comment: C: Why annotations are not encoded using standard informatic format ?
7.4 years ago by User 59 13k
1
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6.0k
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Comment: C: Why mate-Paired end, Paired-end and Single End reads library to be combined for
7.5 years ago by User 59 13k
1
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1
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6.0k
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Comment: C: Why mate-Paired end, Paired-end and Single End reads library to be combined for
7.5 years ago by User 59 13k
1
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0
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2.5k
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Comment: C: Identifying contaminant sources
7.5 years ago by User 59 13k
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0
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4.2k
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Comment: C: fastqc and coverage
7.5 years ago by User 59 13k
1
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0
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3.9k
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Comment: C: Establishing a Core Bioinformatics Facility
7.5 years ago by User 59 13k
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0
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2.1k
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Comment: C: What are the most important unresolved problems in Bioinformatics?
7.6 years ago by User 59 13k
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4.8k
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Comment: C: (Modern, mid-2016) RNA-seq software pipeline
7.6 years ago by User 59 13k
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2
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1.6k
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Comment: C: Use of Bowtie2 in NGS
7.7 years ago by User 59 13k
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2.5k
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Comment: C: Is there any NGS tool which produce long pairwise reads?
7.7 years ago by User 59 13k
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2.5k
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Comment: C: Is there any NGS tool which produce long pairwise reads?
7.7 years ago by User 59 13k
0
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1
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288k
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Comment: C: Gene Id Conversion Tool
7.7 years ago by User 59 13k
0
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1
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3.3k
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Comment: C: Selection between Illumina Hiseq 2500 and NextSeq
7.7 years ago by User 59 13k
1
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0
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1.8k
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Comment: C: Where to compute Support Vector Machines?
7.8 years ago by User 59 13k
0
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0
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3.5k
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Comment: C: Consequences of degraded DNA for Sequencing
7.8 years ago by User 59 13k
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0
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1.3k
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Comment: C: Assign degree of belief according to the evidence code that support the Go annot
7.8 years ago by User 59 13k
1
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0
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1.9k
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Comment: C: variant phred scale of plant genome
7.8 years ago by User 59 13k
0
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1
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1.7k
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Comment: C: Tools for SNP Calling and Assemble sequences from short read files
7.8 years ago by User 59 13k
2
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0
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11k
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Comment: C: Bimodal GC content
7.8 years ago by User 59 13k
0
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0
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4.7k
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Comment: C: How to get per sample read counts/FPKM values from cufflinks?
7.9 years ago by User 59 13k
0
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1
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4.7k
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Comment: C: How to get per sample read counts/FPKM values from cufflinks?
7.9 years ago by User 59 13k
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0
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2.1k
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Comment: C: microRNA microarray or small RNASeq
7.9 years ago by User 59 13k
0
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1
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1.8k
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Comment: C: Whole genome plant sequencing
7.9 years ago by User 59 13k
410 results • Page 1 of 9
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