Off topic:Seeking Collaborators for project
3
2
Entering edit mode
4.6 years ago
elginong1 ▴ 20

THIS IS A SPAM POST posed as a legitimate bioinformatics related question. This is probably the first bioinformatics spam in the history. We are keeping this post as a reference.

Hi,

I am doing an independent research on the current evolutionary patterns of homo sapiens.

I am about to receive the raw FASTQ data of the WGS of a certain individual with unknown or novel mutations. The data might show some pieces of unknown sequences and they cannot be found in any database. The variance is not SNP-based and not seen before in the human populations sequenced to date.

I would like to map the data to the human genome and all other species in the animal kingdom. What is the protocol for further research on the leftover unknown/unusual sequences?

The targeted phenotype of the individual itself is undocumented and unknown, so the chromosomal or genetic mutations are definitely unmappable reads.

Please reply soon

Sincerely,

Elgin Ong

sequence novel Forum • 2.1k views
ADD COMMENT
This thread is not open. No new answers may be added
Traffic: 2530 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6