Erratum to: a SNP profiling panel for sample tracking in whole-exome sequencing studies.

This is an Erratum to Genome Medicine 2013, 5:89, highlighting an error in Table 1 of the original article. Please see related article: http://genomemedicine.com/content/5/9/89.[This corrects the article DOI: 10.1186/gm492.].

Erratum

It has come to our attention that there is an error in Table 1 of our article [1]. Within the ‘Alleles’ column, incorrect reference/alternate nucleotides have been given. This error is limited to this column, all other data and conclusions presented are correct. The corrected Table 1 is shown below.

Table 1

Optimised panel of identifying SNPs

Chromosome	Position a	dbSNP rsID	Gene	Alleles	HapMap 3 AF
					CEU	CHB	JPT	YRI
1	179520506	rs1410592	NPHS2	A/G	0.59	0.62	0.54	0.53
1	67861520	rs2229546	IL12RB2	A/C	0.64	0.36	0.44	0.58
2	169789016	rs497692	ABCB11	A/Gb	0.55	0.65	0.51	0.22
2	227896976	rs10203363	COL4A4	C/T	0.46	0.44	0.36	0.57
3	4403767	rs2819561	SUMF1	C/Tb	0.56	0.73	0.73	0.72
4	5749904	rs4688963	EVC	A/Gb	0.33	0.65	0.67	0.52
5	82834630	rs309557	VCAN	A/Gb	0.49	0.34	0.52	0.50
6	146755140	rs2942	GRM1	A/G	0.54	0.49	0.55	0.47
7	48450157	rs17548783	ABCA13	C/T	0.46	0.72	0.53	0.48
8	94935937	rs4735258	PDP1	C/T	0.40	0.64	0.66	0.46
9	100190780	rs1381532	TDRD7	C/Tb	0.48	0.59	0.50	0.58
10	100219314	rs10883099	HPSE2	A/G	0.52	0.52	0.53	0.62
11	16133413	rs4617548	SOX6	A/G	0.52	0.65	0.61	0.51
12	993930	rs7300444	WNK1	C/T	0.46	0.55	0.48	0.28
13	39433606	rs9532292	FREM2	A/G	0.29	0.41	0.44	0.54
14	50769717	rs2297995	L2HGDH	A/G	0.55	0.65	0.67	0.59
15	34528948	rs4577050	SLC12A6	A/G	0.68	0.75	0.63	0.32
16	70303580	rs2070203	AARS	C/Tb	0.53	0.28	0.51	0.49
17	71197748	rs1037256	COG1	A/G	0.50	0.67	0.65	0.56
18	21413869	rs9962023	LAMA3	C/T	0.67	0.81c	0.75	0.51
19	10267077	rs2228611	DNMT1	A/Gb	0.47	0.73	0.56	0.48
20	6100088	rs10373	FERMT1	C/Tb	0.54	0.31	0.35	0.58
21	44323590	rs4148973	NDUFV3	G/T	0.65	0.33	0.38	0.73
22	21141300	rs4675	SERPIND1	C/T	0.46	0.62	0.51	0.57

aPosition as defined in genome reference assembly GRCh37 (hg19).

bSNP alleles are defined on the negative strand to be consistent with dbSNP.

cAF marginally outside target range for candidate selection. Selected due to paucity of candidates on chromosome 18.