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2
votes
2
replies
966
views
Protein sequence to Nucleotide sequence
linux
awk
codon
sed
perl
updated 3.2 years ago by
Pierre Lindenbaum
164k • written 3.2 years ago by
mittu1602
▴ 200
0
votes
0
replies
3.4k
views
Comment:
Comment: Free codon optimization tools for ordering DNA?
3.2 years ago by
mittu1602
▴ 200
0
votes
0
replies
1.5k
views
Comment:
Comment: whole genome sequence for origami 2 (DE3) and rosetta 2 (DE3)
3.4 years ago by
mittu1602
▴ 200
2
votes
4
replies
1.5k
views
whole genome sequence for origami 2 (DE3) and rosetta 2 (DE3)
ecoli
cells
rosetta2
origami2
competent
Novagen
updated 2.5 years ago by
Sonia
• 0 • written 3.4 years ago by
mittu1602
▴ 200
1
vote
2
replies
2.2k
views
targeted bam file from database for breast cancer
ngs
cancer
targeted
updated 3.9 years ago by
Biostar
20 • written 7.2 years ago by
mittu1602
▴ 200
5
votes
7
replies
3.3k
views
Genome assembly contig ordering
genome
Assembly
updated 5.5 years ago by
Biostar
20 • written 7.5 years ago by
mittu1602
▴ 200
5
votes
4
replies
1.4k
views
save the file_name according to the column headers
microarray
SNP
updated 5.9 years ago by
Biostar
20 • written 7.1 years ago by
mittu1602
▴ 200
0
votes
0
replies
6.6k
views
Answer:
A: Issue converting VCF to MAF using snpEff annotations
6.6 years ago by
mittu1602
▴ 200
0
votes
1
reply
6.3k
views
Answer:
A: How to fix .bam file that was diagnosed as "MISSING_READ_GROUP" by Picard Valida
6.6 years ago by
mittu1602
▴ 200
0
votes
3
replies
2.1k
views
how to annotate chromosome position with the gene list file
Genomics
updated 6.8 years ago by
Paul
★ 1.5k • written 6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
1.9k
views
Comment:
C: No RS id was called in vcf file after giving dbsnp command
6.8 years ago by
mittu1602
▴ 200
1
vote
0
replies
2.3k
views
Genome Studio confusing SNP allele coding schema, what is the main genotype of the sample?
Illumina
genomeStudio
6.8 years ago by
mittu1602
▴ 200
0
votes
0
replies
12k
views
Comment:
C: HOw to merge multifasta sequence into a single sequence having only one header?
6.8 years ago by
mittu1602
▴ 200
3
votes
1
reply
12k
views
Answer:
A: HOw to merge multifasta sequence into a single sequence having only one header?
6.8 years ago by
mittu1602
▴ 200
0
votes
0
replies
2.5k
views
Comment:
C: How to use NCBI Gnomon?
6.9 years ago by
mittu1602
▴ 200
1
vote
2
replies
2.5k
views
Answer:
A: How to use NCBI Gnomon?
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.3k
views
Comment:
C: Matching complementary genotypes from 2 different files
6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
3.0k
views
Comment:
C: Query regarding BLASTKOALA (KEGG) for pathway annotation
6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
2.6k
views
Answer:
A: How to merge two files genotype and ped In Linux? I sample files as follows.
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.3k
views
Comment:
C: Matching complementary genotypes from 2 different files
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
2.4k
views
How can I get other parameters from Ensembl VEP for vcf annotation
variant type
snps
6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
2.4k
views
Comment:
C: How can I get other parameters from Ensembl VEP for vcf annotation
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.3k
views
Comment:
C: Matching complementary genotypes from 2 different files
6.9 years ago by
mittu1602
▴ 200
1
vote
1
reply
1.4k
views
Answer:
A: scaffold builder - parameters and output analysis
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.3k
views
Comment:
C: Matching complementary genotypes from 2 different files
6.9 years ago by
mittu1602
▴ 200
3
votes
9
replies
1.3k
views
Matching complementary genotypes from 2 different files
genomics
updated 6.9 years ago by
Kevin Blighe
88k • written 6.9 years ago by
mittu1602
▴ 200
2
votes
1
reply
1.3k
views
argyle: an R package for analysis of Illumina genotyping arrays
R
6.9 years ago by
mittu1602
▴ 200
2
votes
1
reply
2.2k
views
VARScan2 Error, CBS segmentation by "DNACopy"
R
CNV
updated 6.9 years ago by
Kevin Blighe
88k • written 6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
3.5k
views
Comment:
C: VarScan-Somatic Copy Number Alteration (CNA) Calling
6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
2.1k
views
Comment:
C: how to annotate chromosome position with the gene list file
6.9 years ago by
mittu1602
▴ 200
1
vote
0
replies
4.3k
views
Answer:
A: how to grep word with hyphen/dash of A file in one column of B file
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
3.5k
views
Comment:
C: VarScan-Somatic Copy Number Alteration (CNA) Calling
6.9 years ago by
mittu1602
▴ 200
2
votes
0
replies
4.5k
views
Answer:
A: blastx results: small letters with gray color?
6.9 years ago by
mittu1602
▴ 200
0
votes
1
reply
3.5k
views
Comment:
C: VarScan-Somatic Copy Number Alteration (CNA) Calling
6.9 years ago by
mittu1602
▴ 200
0
votes
0
replies
3.5k
views
Comment:
C: VarScan-Somatic Copy Number Alteration (CNA) Calling
6.9 years ago by
mittu1602
▴ 200
1
vote
1
reply
1.4k
views
varscan copy number error
varscan
cnv
7.0 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.8k
views
Comment:
C: Varscan copynumber running problem
7.0 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.5k
views
Answer:
A: making grep method specific in perl
7.0 years ago by
mittu1602
▴ 200
0
votes
0
replies
3.6k
views
Comment:
C: vcftools keep only indels not working
7.0 years ago by
mittu1602
▴ 200
0
votes
1
reply
4.8k
views
Comment:
C: BWA-mem alignment is not giving desired output
7.0 years ago by
mittu1602
▴ 200
2
votes
0
replies
1.5k
views
Comment:
C: Tophat 2 error
7.0 years ago by
mittu1602
▴ 200
0
votes
0
replies
2.9k
views
Comment:
C: Detect CNVs in single sample using cn.MOPS
7.0 years ago by
mittu1602
▴ 200
1
vote
1
reply
4.8k
views
Answer:
A: BWA-mem alignment is not giving desired output
7.0 years ago by
mittu1602
▴ 200
1
vote
1
reply
3.7k
views
Answer:
A: sam to bam conversion problem
7.0 years ago by
mittu1602
▴ 200
0
votes
1
reply
3.7k
views
Comment:
C: sam to bam conversion problem
7.0 years ago by
mittu1602
▴ 200
3
votes
1
reply
3.3k
views
Why GC-content normalization for CNV analysis?
cnv
ngs
illumina
updated 7.0 years ago by
Jan Oosting
▴ 920 • written 7.0 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.4k
views
Comment:
C: How to normalize and pool normal human samples?
7.0 years ago by
mittu1602
▴ 200
1
vote
3
replies
1.4k
views
How to normalize and pool normal human samples?
ngs
illumina
7.0 years ago by
mittu1602
▴ 200
0
votes
2
replies
1.6k
views
Comment:
C: determine overlaps of chromosome coordinates from two different files
7.1 years ago by
mittu1602
▴ 200
0
votes
1
reply
1.6k
views
Comment:
C: determine overlaps of chromosome coordinates from two different files
7.1 years ago by
mittu1602
▴ 200
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