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Comment:
Comment: Convert genomic files from known Gigabases(# of bases) to gigabytes
2.7 years ago by
Ram
45k
2
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1
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2.1k
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Answer:
Answer: RSEM calculate-expression has only one sample in .isoforms.results file
2.7 years ago by
Ram
45k
0
votes
1
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3.7k
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Comment:
Comment: convert single bam file to VCF format
2.7 years ago by
Ram
45k
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0
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3.7k
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Comment:
Comment: convert single bam file to VCF format
2.7 years ago by
Ram
45k
1
vote
1
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1.2k
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Comment:
Comment: Convert genomic files from known Gigabases(# of bases) to gigabytes
2.7 years ago by
Ram
45k
0
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1
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1.3k
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Comment:
Comment: R error
2.7 years ago by
Ram
45k
0
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0
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4.5k
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Comment:
Comment: Generating count matrix for STAR counts in GDC v32.0 for RNA-Seq
2.7 years ago by
Ram
45k
0
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0
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1.3k
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Comment:
Comment: Error while converting ExpressionSet format to SingleCellExperiment format?
2.7 years ago by
Ram
45k
1
vote
0
replies
4.0k
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Comment:
Comment: Extracting gapped sequences from Bio.Align.PairwiseAligner
2.7 years ago by
Ram
45k
0
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1
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1.3k
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Comment:
Comment: Error while converting ExpressionSet format to SingleCellExperiment format?
2.7 years ago by
Ram
45k
0
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0
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8.7k
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Comment:
Comment: Encountering error when loading scanpy?
2.7 years ago by
Ram
45k
0
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0
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2.5k
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Comment:
Comment: When I run Trimmomatic, I continue to get an "unknown trimmer" error and cannot
2.7 years ago by
Ram
45k
1
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0
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4.0k
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Comment:
Comment: Extracting gapped sequences from Bio.Align.PairwiseAligner
2.7 years ago by
Ram
45k
1
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0
replies
2.1k
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Comment:
Comment: How to fix "Contig chrKI270728.1 not present in the sequence dictionary " error
2.7 years ago by
Ram
45k
1
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1
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2.5k
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Comment:
Comment: Data from an experiment
2.7 years ago by
Ram
45k
1
vote
1
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2.5k
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Comment:
Comment: Data from an experiment
2.7 years ago by
Ram
45k
1
vote
1
reply
2.1k
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Comment:
Comment: How to fix "Contig chrKI270728.1 not present in the sequence dictionary " error
2.7 years ago by
Ram
45k
1
vote
0
replies
4.0k
views
Comment:
Comment: Extracting gapped sequences from Bio.Align.PairwiseAligner
2.7 years ago by
Ram
45k
0
votes
0
replies
1.9k
views
Comment:
Comment: Sum the values based on the variant names and give the result in stats format
2.7 years ago by
Ram
45k
0
votes
1
reply
4.4k
views
Comment:
Comment: Can't liftover vcf file from hg19 to hg38
2.7 years ago by
Ram
45k
0
votes
0
replies
1.9k
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Comment:
Comment: Sum the values based on the variant names and give the result in stats format
2.7 years ago by
Ram
45k
0
votes
1
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1.9k
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Comment:
Comment: Sum the values based on the variant names and give the result in stats format
2.7 years ago by
Ram
45k
0
votes
1
reply
4.4k
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Comment:
Comment: Can't liftover vcf file from hg19 to hg38
2.7 years ago by
Ram
45k
0
votes
1
reply
1.9k
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Comment:
Comment: Sum the values based on the variant names and give the result in stats format
2.7 years ago by
Ram
45k
0
votes
1
reply
4.4k
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Comment:
Comment: Can't liftover vcf file from hg19 to hg38
2.7 years ago by
Ram
45k
0
votes
1
reply
4.4k
views
Comment:
Comment: Can't liftover vcf file from hg19 to hg38
2.7 years ago by
Ram
45k
0
votes
0
replies
1.8k
views
Comment:
Comment: extract pattern using grep/sed
2.7 years ago by
Ram
45k
0
votes
1
reply
1.9k
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Comment:
Comment: Sum the values based on the variant names and give the result in stats format
2.7 years ago by
Ram
45k
0
votes
0
replies
74k
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Comment:
Comment: Sequence Number Count In Fastq.Gz File
2.7 years ago by
Ram
45k
0
votes
0
replies
979
views
Comment:
Comment: how to change >header in to new line??
2.7 years ago by
Ram
45k
0
votes
0
replies
2.0k
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Comment:
Comment: Extract gene sequences from multiple fasta using a list from a file:
2.7 years ago by
Ram
45k
0
votes
0
replies
29k
views
Comment:
Comment: intersect VCF files
2.7 years ago by
Ram
45k
0
votes
0
replies
2.0k
views
Comment:
Comment: Extract gene sequences from multiple fasta using a list from a file:
2.7 years ago by
Ram
45k
0
votes
0
replies
1.8k
views
Comment:
Comment: Error with indexing! STAR unable to access genome file SOS
2.7 years ago by
Ram
45k
0
votes
0
replies
1.8k
views
Comment:
Comment: Linux command to edit CHROM column in VCF file
2.7 years ago by
Ram
45k
0
votes
1
reply
2.0k
views
Comment:
Comment: Extract gene sequences from multiple fasta using a list from a file:
2.7 years ago by
Ram
45k
0
votes
0
replies
6.0k
views
Comment:
Comment: Sort gff3 on chromosome, position and then featuretype (gene, mRNA, exon, CDS)
2.7 years ago by
Ram
45k
0
votes
1
reply
29k
views
Comment:
Comment: intersect VCF files
2.7 years ago by
Ram
45k
0
votes
1
reply
29k
views
Comment:
Comment: intersect VCF files
2.7 years ago by
Ram
45k
0
votes
0
replies
5.5k
views
Comment:
Comment: Any database on cancer related snp information
2.7 years ago by
Ram
45k
0
votes
0
replies
1.1k
views
Comment:
Comment: Virtual box
2.7 years ago by
Ram
45k
0
votes
0
replies
33k
views
Comment:
Comment: Translating gene names to entrez id's
2.7 years ago by
Ram
45k
0
votes
0
replies
2.5k
views
Comment:
Comment: RNAseq for DE purpose
2.7 years ago by
Ram
45k
0
votes
1
reply
2.5k
views
Comment:
Comment: RNAseq for DE purpose
2.7 years ago by
Ram
45k
0
votes
1
reply
2.5k
views
Comment:
Comment: RNAseq for DE purpose
2.7 years ago by
Ram
45k
0
votes
1
reply
2.5k
views
Comment:
Comment: RNAseq for DE purpose
2.7 years ago by
Ram
45k
0
votes
0
replies
1.5k
views
Comment:
Comment: Change accession number to chromosome number in reference genome
2.7 years ago by
Ram
45k
0
votes
0
replies
1.8k
views
Comment:
Comment: How to change every third line in a fastq library
2.7 years ago by
Ram
45k
1
vote
0
replies
1.8k
views
Answer:
Answer: How to change every third line in a fastq library
2.7 years ago by
Ram
45k
0
votes
0
replies
876
views
Comment:
Comment: Where can I get the ICB datasets in this website?
2.7 years ago by
Ram
45k
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