Skip to main content
. 2012 May 10;13:177. doi: 10.1186/1471-2164-13-177

Table 2.

tSMS sequencing of ancient DNA extracts from sample TP (13,389 ± 52BP)

Sample Platform # Conditions #Seqs nucDNA bp mtDNA bp %Endo.
TP1
110 V
1
80°C, Phosphatase
1,980,210
85,738
2,885,229
53
1,845
4.33%
 
110 V
1
80°C
234,094
28,797
998,007
8
255
12.30%
 
110 V
1
95°C
228,871
12,573
438,111
5
162
5.50%
TP1RE
110 V
1
80°C, Phosphatase
1,607,848
161,284
5,597,277
99
3,378
10.04%
 
550 V
8
80°C, Phosphatase
16,290,720
1,480,012
46,444,135
935
29,637
9.09%
 
110 V
1
80°C
214,070
48,304
1,718,507
29
991
22.58%
 
110 V
1
95°C
356,586
51,052
1,798,348
31
1,169
14.33%
TP2
110 V
1
80°C, Phosphatase
2,088,705
177,944
6,147,860
50
1,713
8.52%
 
110 V
1
80°C
216,159
53,463
1,879,011
16
560
24.74%
 
110 V
1
95°C
354,155
62,259
2,170,975
15
516
17.58%
TP2RE
110 V
1
80°C, Phosphatase
233,613
32,045
1,094,783
10
318
13.72%
 
110 V
1
80°C
213,958
59,530
2,072,120
26
928
27.84%
  110 V 1 95°C 247,784 55,848 1,939,018 22 781 22.55%

Sample TP was extracted in duplicate, and identical volumes of the extracts were tSMS sequenced on Helicos 110 FOV channels following different template preparation procedures as described in the methods section. The total number of sequences (#Seqs) as well as the number of hits mapping the horse reference nuclear (nucDNA) and mitochondrial (mtDNA) genome with mapping qualities higher than 25 but with no hit on the human reference genomes hg19 and rCRS are reported. The total sequence length covered by these reads is indicated in bp. The fraction of endogenous reads is estimated by summing the number of reads identified in nucDNA and mtDNA and dividing by the total number of reads generated per channel.