User: bulbul
bulbul • 10
- Reputation:
- 10
- Status:
- New User
- Location:
- Last seen:
- 1 year, 1 month ago
- Joined:
- 3 years, 7 months ago
- Email:
- b*****@iasri.res.in
Posts by bulbul
<prev
• 9 results •
page 1 of 1 •
next >
0
votes
0
answers
309
views
0
answers
... How to convert DArT file containing binary (0, 1) into AT,GC format. Kindly suggest it ...
written 13 months ago by
bulbul • 10
0
votes
0
answers
220
views
0
answers
... CloneID Sequence CloneID P1 P2 1 2 3 4
11061 TCGCTGTACACTGTTGACGTCGCC 11061 1 1 1 1 1 1
11294 AAAGGTTCTATCTCGCTGAAACCCAG 11294 0 1 1 1 1 1
22912 ACCATCGCTGCACCACCTTGACCT 22912 1 - 1 1 1 1
11324 AGCAGCGTCGACTGCCGAGATCGG ...
0
votes
0
answers
396
views
0
answers
Comment:
C: conversion binary to ATGC
... "0" = Reference allele homozygote, "1"= SNP allele homozygote, "-" = missing. But I do not know to to convert the above example data into AT GC AA CC like. kindly suggest me. thank you. ...
written 13 months ago by
bulbul • 10
1
vote
0
answers
396
views
0
answers
... CloneID Sequence CloneID P1 P2 1 2 3 4
11061 TCGCTGTACACTGTTGACGTCGCC 11061 1 1 1 1 1 1
11294 AAAGGTTCTATCTCGCTGAAACCCAG 11294 0 1 1 1 1 1
22912 ACCATCGCTGCACCACCTTGACCT 22912 1 - 1 1 1 1
11324 AGCAGCGTCGACTGCCGAGATCGG ...
written 13 months ago by
bulbul • 10
• updated
13 months ago by
lakhujanivijay ♦ 4.6k
1
vote
1
answer
360
views
1
answer
... How to find out the chromosome position of each sequence of the sample?
Thanks in advance
Sequence CloneID Chromosome ChromosomePosition
TGCAGTTATTTGGCTCATCGTCGTATTGCAAGTTTCTGACATCGCTGTACACTGTTGACGTCGCCGAGA 1106145|F|0 contig103705_ln_2374_nr_121_ 2005
TGCAGGGCCGCCATGCCACCGAGTCTGGCGTG ...
0
votes
0
answers
301
views
0
answers
... I have install docker and python which are dependent tools as these are dependent tools. Can any body tell me how to install **furious-luke/lizards-are-awesome** in Ubuntu as i tried through the instruction on https://github.com/furious-luke/lizards-are-awesome. I dont know how to install **furious- ...
written 14 months ago by
bulbul • 10
0
votes
3
answers
1.8k
views
3
answers
... how shoulld i pull out the mutiple sequences from one fasta file by using gene id header in another text file?? what is command use in linux? ...
written 3.6 years ago by
bulbul • 10
4
votes
2
answers
864
views
2
answers
... I have a de novo assembly file "denovo.fasta", and another file with 25,000 genes id "gene_id.txt". how should i retrive those sequences from the "denovo.fasta" which are only present in "gene_id.txt" file? ...
0
votes
1
answer
877
views
1
answer
... i have six files. each file have lakhs of gene_id. i have to find out all the genes that are present in all file. if any gene(s) is/are not present even in a single file. then i have to delete them. how should i do it?? ...
written 3.6 years ago by
bulbul • 10
• updated
3.6 years ago by
natasha.sernova • 3.7k
Latest awards to bulbul
No awards yet. Soon to come :-)
Use of this site constitutes acceptance of our User
Agreement
and Privacy
Policy.
Powered by Biostar
version 2.3.0
Traffic: 906 users visited in the last hour