This is a test version of Biostars. For the public version, visit https://www.biostars.org.
Novel Sequence Insertions 1000 Genomes Project

I am looking for novel sequence insertions identified in the 1000 genomes project, and I found 3 files in this directory:

ftp://ftp.ebi.ac.uk/pub/databases/dgva/estd59_Durbin_et_al_2010/gvf/estd59_Durbin_2010_highquality_novel_sequence_insertion_pilot2.gvf
ftp://ftp.ebi.ac.uk/pub/databases/dgva/estd59_Durbin_et_al_2010/gvf/estd59_Durbin_2010_highquality_mobile_element_insertion_pilot1.gvf
ftp://ftp.ebi.ac.uk/pub/databases/dgva/estd59_Durbin_et_al_2010/gvf/estd59_Durbin_2010_highquality_mobile_element_insertion_pilot2.gvf

It seems for non-mobile element insertions, there is only about 400 novel sequence insertions. Is there any other place where I can find more?

EDIT: for mobile elements, Casey Bergman's answer seems to be the best out there. Still, out of 7830 entries in the table, only 3089 sequences are given for the predictions in this table, the rest being blank.

genome indel

Mobile element insertions are not novel.

Neither are segmental duplications or CNVs for that matter. Virtually all new sequence come from pre-exisiting sequences in the genome. I think "novel" here is shorthand "not in the reference genome".

I believe the SV people has a consensus about how to define "novel". Even paper I read on "novel" sequences/insertions define "novel" essentially the same way.

I believe the SV people has a consensus about how to define "novel". Every paper I read on "novel" sequences/insertions define "novel" essentially the same way.

2 answers

Look in Table S1 of Stewart et al (2011) A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans: http://www.plosgenetics.org/article/info%3Adoi/10.1371/journal.pgen.1002236

If so, then I would amend your question to clearly state that you are looking for non-mobile element sequences.

In the 1000G pilot paper (A map of human genome variation from population-scale sequencing. The 1000 Genomes Consortium. Nature 467,1061-73 (2010)), we assembled 164 humans with Cortex and assembled novel sequence. The file is here:

ftp.1000genomes.ebi.ac.uk:/vol1/ftp/pilot_data/paper_data_sets/a_map_of_human_variation/low_coverage/sv/low_coverage.2010_10.novel_sequence

and the method is explained in the Supp Info.

Log in to answer this question.