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Comment: C: How can I get only the rows when for the converge points : - +
7.1 years ago by cpad0112 21k
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2.1k
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Comment: C: Extraction of read subsequences based on a region from a sam file
7.1 years ago by cpad0112 21k
2
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2
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2.8k
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Answer: C: How can I get only the rows when for the converge points : - +
7.1 years ago by cpad0112 21k
0
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1
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2.1k
views
Comment: C: Extraction of read subsequences based on a region from a sam file
7.1 years ago by cpad0112 21k
1
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1
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1.9k
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Comment: C: What counts as "complex code"?
7.1 years ago by cpad0112 21k
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2
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5.7k
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Comment: C: Are these two proteins homolog?
7.1 years ago by cpad0112 21k
3
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0
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1.9k
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Comment: C: What counts as "complex code"?
7.1 years ago by cpad0112 21k
0
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0
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3.4k
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Comment: C: Extracting Bar code From Fastq file
7.1 years ago by cpad0112 21k
1
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1
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4.3k
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Comment: C: Extract start coordinate from read 1 and end coordinate from read 2 of paired en
7.1 years ago by cpad0112 21k
0
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1
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1.7k
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Comment: C: how to find the locations of protein products of a certain list of genes?
7.1 years ago by cpad0112 21k
1
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1
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4.3k
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Comment: C: Extract start coordinate from read 1 and end coordinate from read 2 of paired en
7.1 years ago by cpad0112 21k
2
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2
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4.3k
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Answer: C: Extract start coordinate from read 1 and end coordinate from read 2 of paired en
7.1 years ago by cpad0112 21k
0
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0
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3.2k
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Comment: C: how merge the gene expression value of two sample
7.1 years ago by cpad0112 21k
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0
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3.1k
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Comment: C: chromosome coordinate, rs
7.1 years ago by cpad0112 21k
0
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1
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3.1k
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Comment: C: chromosome coordinate, rs
7.1 years ago by cpad0112 21k
3
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2
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12k
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Comment: C: Cat command to combine multiple fastq.gz file
7.1 years ago by cpad0112 21k
1
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1
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4.5k
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Comment: C: Subset of genes with at least 1 intron larger than 5000 kbp
7.1 years ago by cpad0112 21k
0
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0
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1.7k
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Comment: C: How to add sequence information to vcf from MPileup
7.1 years ago by cpad0112 21k
0
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0
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1.7k
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Comment: C: How to add sequence information to vcf from MPileup
7.1 years ago by cpad0112 21k
0
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0
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7.5k
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Comment: C: Count number of SNPs per chromosome in vcf file
7.1 years ago by cpad0112 21k
0
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1
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11k
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Comment: C: bcftools variant filteration
7.1 years ago by cpad0112 21k
0
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0
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7.5k
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Comment: C: calculate SNP in raw vcf file
7.1 years ago by cpad0112 21k
0
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1
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9.4k
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Comment: C: how to visualize co-expression of several genes simultaneously in Featureplot (s
7.1 years ago by cpad0112 21k
0
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1
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9.4k
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Comment: C: how to plot several gene in Featureplot(scRNA-seq) simultaneously?
7.1 years ago by cpad0112 21k
0
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1
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4.9k
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Comment: C: While using ggtree in rstudio, it shows error in some commands
7.1 years ago by cpad0112 21k
1
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0
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1.5k
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Comment: C: Semicolon vs vertical line separating GO annotations in .go file
7.1 years ago by cpad0112 21k
1
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1
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4.3k
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Comment: C: seqtk subseq command not pulling full fastq reads
7.1 years ago by cpad0112 21k
0
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0
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2.6k
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Comment: C: Use Read ID File to parse out reads from a Fasta File
7.1 years ago by cpad0112 21k
0
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0
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3.5k
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Comment: C: Tool that can split genes into groups with similar expression pattern overtime
7.1 years ago by cpad0112 21k
0
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0
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4.9k
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Comment: C: While using ggtree in rstudio, it shows error in some commands
7.1 years ago by cpad0112 21k
0
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1
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2.6k
views
Answer: C: Use Read ID File to parse out reads from a Fasta File
7.1 years ago by cpad0112 21k
0
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1
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3.5k
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Comment: C: Tool that can split genes into groups with similar expression pattern overtime
7.1 years ago by cpad0112 21k
0
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1
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3.5k
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Comment: C: Tool that can split genes into groups with similar expression pattern overtime
7.1 years ago by cpad0112 21k
0
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1
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2.2k
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Comment: C: SNPs genomic classification based on VCF annotation
7.1 years ago by cpad0112 21k
0
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1
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2.7k
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Comment: C: Allele counting tool for a list of known indels from paired end sequencing data
7.1 years ago by cpad0112 21k
0
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1
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10k
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Comment: C: Rsubread: Aligning multiple paired-end files
7.1 years ago by cpad0112 21k
0
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1
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10k
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Comment: C: Rsubread: Aligning multiple paired-end files
7.1 years ago by cpad0112 21k
1
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1
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10k
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Comment: C: Rsubread: Aligning multiple paired-end files
7.1 years ago by cpad0112 21k
0
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1
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2.7k
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Comment: C: Allele counting tool for a list of known indels from paired end sequencing data
7.1 years ago by cpad0112 21k
0
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1
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2.7k
views
Comment: C: Allele counting tool for a list of known indels from paired end sequencing data
7.1 years ago by cpad0112 21k
0
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1
reply
2.7k
views
Comment: C: Allele counting tool for a list of known indels from paired end sequencing data
7.1 years ago by cpad0112 21k
0
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0
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2.5k
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Comment: C: How to find genomic coordinates of specific deletion in the HR gene?
7.1 years ago by cpad0112 21k
1
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0
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13k
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Comment: C: GSEA, input metrics
7.1 years ago by cpad0112 21k
0
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0
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13k
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Comment: C: GSEA, input metrics
7.1 years ago by cpad0112 21k
0
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0
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3.3k
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Comment: C: Search for gene variants
7.1 years ago by cpad0112 21k
0
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1
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2.2k
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Comment: C: SNPs genomic classification based on VCF annotation
7.1 years ago by cpad0112 21k
0
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0
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1.8k
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Comment: C: Struggle with awk command
7.1 years ago by cpad0112 21k
2
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1
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2.2k
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Answer: C: SNPs genomic classification based on VCF annotation
7.1 years ago by cpad0112 21k
0
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0
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25k
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Comment: C: How to convert fasta file format to phylip file format
7.1 years ago by cpad0112 21k
0
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0
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25k
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Comment: C: How to convert fasta file format to phylip file format
7.1 years ago by cpad0112 21k
3,458 results • Page 41 of 70
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