Hi Ya,

You can refer to the track description page for more information on the 
Neanderthal Sequence Contigs: 
http://genome.ucsc.edu/cgi-bin/hgTrackUi?g=ntSeqContigs&db=panTro2

Please contact us again at [email protected] if you have any further 
questions.

---
Luvina Guruvadoo
UCSC Genome Bioinformatics Group


On 7/1/2011 7:50 AM, Ya Hu wrote:
> Dear sir or madam,
>
> I currently downloaded Neanderthal sequence contigs from:
>
> ftp://hgdownload.cse.ucsc.edu/gbdb/panTro2/neandertal/seqAlis/all-pt2.bam
>
> >From original paper (Green et al. 2010) one section describes further
> processing of Neanderthal sequences as:
>
>
> 1. We required that all reads map to the PanTro2 chimpanzee genome sequence.
>
> 2. We required there to be no insertion/deletion polymorphisms when aligned
> to chimpanzee.
>
> 3. We restricted to autosomal reads.
>
> 4. We required that no more than 10% of bases in the reads disagree with
> chimpanzee.
>
> 5. We only accepted nucleotides with a map quality (MAPQ) of at least 43 as
> assessed by the ANFO
>
> software, which is specialized for mapping ancient DNA reads (
>
> *S13*).
>
> 6. We did not analyze nucleotides within 5bp of either end of the Neandertal
> read, because it is known
>
> that sequence quality is lower in these regions (
>
> *S28*).
>
>
>
> Please ask whether current Neanderthal data are results of above processes?
>
> Many thanks,
>
> Ya
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>   

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