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2
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2
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1.0k
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Protein sequence to Nucleotide sequence
linux awk codon sed perl
updated 3.5 years ago by 165k • written 3.5 years ago by ▴ 200
0
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0
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3.6k
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Comment: Comment: Free codon optimization tools for ordering DNA?
3.5 years ago by mittu1602 ▴ 200
0
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0
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1.7k
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Comment: Comment: whole genome sequence for origami 2 (DE3) and rosetta 2 (DE3)
3.7 years ago by mittu1602 ▴ 200
2
votes
4
replies
1.7k
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whole genome sequence for origami 2 (DE3) and rosetta 2 (DE3)
ecoli cells rosetta2 origami2 competent Novagen
updated 2.8 years ago by • 0 • written 3.7 years ago by ▴ 200
1
vote
2
replies
2.2k
views
targeted bam file from database for breast cancer
ngs cancer targeted
updated 4.3 years ago by 20 • written 7.5 years ago by ▴ 200
5
votes
7
replies
3.4k
views
Genome assembly contig ordering
genome Assembly
updated 5.8 years ago by 20 • written 7.8 years ago by ▴ 200
5
votes
4
replies
1.5k
views
save the file_name according to the column headers
microarray SNP
updated 6.2 years ago by 20 • written 7.4 years ago by ▴ 200
0
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0
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6.8k
views
Answer: A: Issue converting VCF to MAF using snpEff annotations
6.9 years ago by mittu1602 ▴ 200
0
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1
reply
6.6k
views
Answer: A: How to fix .bam file that was diagnosed as "MISSING_READ_GROUP" by Picard Valida
6.9 years ago by mittu1602 ▴ 200
0
votes
3
replies
2.2k
views
how to annotate chromosome position with the gene list file
Genomics
updated 7.1 years ago by ★ 1.5k • written 7.2 years ago by ▴ 200
0
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0
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2.0k
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Comment: C: No RS id was called in vcf file after giving dbsnp command
7.1 years ago by mittu1602 ▴ 200
1
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0
replies
2.3k
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Genome Studio confusing SNP allele coding schema, what is the main genotype of the sample?
Illumina genomeStudio
7.1 years ago by mittu1602 ▴ 200
0
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0
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13k
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Comment: C: HOw to merge multifasta sequence into a single sequence having only one header?
7.1 years ago by mittu1602 ▴ 200
3
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1
reply
13k
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Answer: A: HOw to merge multifasta sequence into a single sequence having only one header?
7.1 years ago by mittu1602 ▴ 200
0
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0
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2.6k
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Comment: C: How to use NCBI Gnomon?
7.2 years ago by mittu1602 ▴ 200
1
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2
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2.6k
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Answer: A: How to use NCBI Gnomon?
7.2 years ago by mittu1602 ▴ 200
0
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1
reply
1.4k
views
Comment: C: Matching complementary genotypes from 2 different files
7.2 years ago by mittu1602 ▴ 200
0
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0
replies
3.2k
views
Comment: C: Query regarding BLASTKOALA (KEGG) for pathway annotation
7.2 years ago by mittu1602 ▴ 200
0
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0
replies
2.6k
views
Answer: A: How to merge two files genotype and ped In Linux? I sample files as follows.
7.2 years ago by mittu1602 ▴ 200
0
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1
reply
1.4k
views
Comment: C: Matching complementary genotypes from 2 different files
7.2 years ago by mittu1602 ▴ 200
0
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1
reply
2.4k
views
How can I get other parameters from Ensembl VEP for vcf annotation
variant type snps
7.2 years ago by mittu1602 ▴ 200
0
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0
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2.4k
views
Comment: C: How can I get other parameters from Ensembl VEP for vcf annotation
7.2 years ago by mittu1602 ▴ 200
0
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1
reply
1.4k
views
Comment: C: Matching complementary genotypes from 2 different files
7.2 years ago by mittu1602 ▴ 200
1
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1
reply
1.5k
views
Answer: A: scaffold builder - parameters and output analysis
7.2 years ago by mittu1602 ▴ 200
0
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1
reply
1.4k
views
Comment: C: Matching complementary genotypes from 2 different files
7.2 years ago by mittu1602 ▴ 200
3
votes
9
replies
1.4k
views
Matching complementary genotypes from 2 different files
genomics
updated 7.2 years ago by 89k • written 7.2 years ago by ▴ 200
2
votes
1
reply
1.4k
views
argyle: an R package for analysis of Illumina genotyping arrays
R
7.2 years ago by mittu1602 ▴ 200
2
votes
1
reply
2.3k
views
VARScan2 Error, CBS segmentation by "DNACopy"
R CNV
updated 7.2 years ago by 89k • written 7.2 years ago by ▴ 200
0
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0
replies
3.7k
views
Comment: C: VarScan-Somatic Copy Number Alteration (CNA) Calling
7.2 years ago by mittu1602 ▴ 200
0
votes
0
replies
2.2k
views
Comment: C: how to annotate chromosome position with the gene list file
7.2 years ago by mittu1602 ▴ 200
1
vote
0
replies
4.6k
views
Answer: A: how to grep word with hyphen/dash of A file in one column of B file
7.2 years ago by mittu1602 ▴ 200
0
votes
1
reply
3.7k
views
Comment: C: VarScan-Somatic Copy Number Alteration (CNA) Calling
7.2 years ago by mittu1602 ▴ 200
2
votes
0
replies
4.9k
views
Answer: A: blastx results: small letters with gray color?
7.2 years ago by mittu1602 ▴ 200
0
votes
1
reply
3.7k
views
Comment: C: VarScan-Somatic Copy Number Alteration (CNA) Calling
7.2 years ago by mittu1602 ▴ 200
0
votes
0
replies
3.7k
views
Comment: C: VarScan-Somatic Copy Number Alteration (CNA) Calling
7.2 years ago by mittu1602 ▴ 200
1
vote
1
reply
1.4k
views
varscan copy number error
varscan cnv
7.3 years ago by mittu1602 ▴ 200
0
votes
1
reply
1.8k
views
Comment: C: Varscan copynumber running problem
7.3 years ago by mittu1602 ▴ 200
0
votes
1
reply
1.6k
views
Answer: A: making grep method specific in perl
7.3 years ago by mittu1602 ▴ 200
0
votes
0
replies
3.6k
views
Comment: C: vcftools keep only indels not working
7.3 years ago by mittu1602 ▴ 200
0
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1
reply
5.0k
views
Comment: C: BWA-mem alignment is not giving desired output
7.3 years ago by mittu1602 ▴ 200
2
votes
0
replies
1.6k
views
Comment: C: Tophat 2 error
7.3 years ago by mittu1602 ▴ 200
0
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0
replies
2.9k
views
Comment: C: Detect CNVs in single sample using cn.MOPS
7.3 years ago by mittu1602 ▴ 200
1
vote
1
reply
5.0k
views
Answer: A: BWA-mem alignment is not giving desired output
7.3 years ago by mittu1602 ▴ 200
1
vote
1
reply
3.9k
views
Answer: A: sam to bam conversion problem
7.3 years ago by mittu1602 ▴ 200
0
votes
1
reply
3.9k
views
Comment: C: sam to bam conversion problem
7.3 years ago by mittu1602 ▴ 200
3
votes
1
reply
3.4k
views
Why GC-content normalization for CNV analysis?
cnv ngs illumina
updated 7.3 years ago by ▴ 920 • written 7.3 years ago by ▴ 200
0
votes
1
reply
1.4k
views
Comment: C: How to normalize and pool normal human samples?
7.3 years ago by mittu1602 ▴ 200
1
vote
3
replies
1.4k
views
How to normalize and pool normal human samples?
ngs illumina
7.3 years ago by mittu1602 ▴ 200
0
votes
2
replies
1.7k
views
Comment: C: determine overlaps of chromosome coordinates from two different files
7.4 years ago by mittu1602 ▴ 200
0
votes
1
reply
1.7k
views
Comment: C: determine overlaps of chromosome coordinates from two different files
7.4 years ago by mittu1602 ▴ 200
86 results • Page 1 of 2
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