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Explore HG002 comparison results

Use this interactive explorer to filter all results across submission entries and multiple dimensions.

Entry	Type	Subtype	Subset	Genotype	F-score	Recall	Precision	Frac_NA	Truth TP	Truth FN	Query TP	Query FP	FP gt	% FP ma

« 1 2 ... 654 655 656 657 658 659 660 661 662 ... 1720 1721 » 32851-32900 / 86044 show all
eyeh-varpipe	INDEL	*	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged	hetalt	73.2771	59.8485	94.4751	88.1311	79	53	171	10	9	90.0000
ckim-gatk	SNP	*	tech_badpromoters	homalt	98.1366	98.7500	97.5309	47.0588	79	1	79	2	2	100.0000
ckim-isaac	INDEL	*	map_l150_m0_e0	homalt	64.7541	48.1707	98.7500	85.5596	79	85	79	1	0	0.0000
cchapple-custom	INDEL	I1_5	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged	homalt	91.1652	96.3415	86.5169	61.6379	79	3	77	12	12	100.0000
cchapple-custom	SNP	*	tech_badpromoters	homalt	98.7421	98.7500	98.7342	44.3662	79	1	78	1	1	100.0000
ciseli-custom	SNP	ti	tech_badpromoters	*	86.2240	92.9412	80.4124	43.9306	79	6	78	19	1	5.2632
ckim-dragen	INDEL	D16_PLUS	map_l100_m1_e0	*	82.7225	90.8046	75.9615	95.2140	79	8	79	25	4	16.0000
ckim-dragen	INDEL	D6_15	map_l150_m2_e0	*	96.9325	96.3415	97.5309	93.1646	79	3	79	2	0	0.0000
ckim-dragen	SNP	*	tech_badpromoters	homalt	98.1366	98.7500	97.5309	47.4026	79	1	79	2	2	100.0000
ndellapenna-hhga	INDEL	D16_PLUS	map_l100_m2_e1	*	83.7401	81.4433	86.1702	87.8866	79	18	81	13	6	46.1538
ndellapenna-hhga	INDEL	D6_15	map_l150_m2_e1	*	94.6730	92.9412	96.4706	91.2281	79	6	82	3	2	66.6667
qzeng-custom	INDEL	I6_15	map_siren	homalt	77.8370	87.7778	69.9187	73.1441	79	11	86	37	1	2.7027
mlin-fermikit	INDEL	*	lowcmp_SimpleRepeat_homopolymer_gt10	*	69.4864	63.7097	76.4151	99.9162	79	45	81	25	24	96.0000
mlin-fermikit	INDEL	D1_5	lowcmp_SimpleRepeat_diTR_51to200	het	41.1619	58.5185	31.7460	42.9003	79	56	60	129	126	97.6744
mlin-fermikit	INDEL	D1_5	map_l250_m2_e0	*	56.5892	42.9348	82.9787	91.5996	79	105	78	16	14	87.5000
mlin-fermikit	INDEL	D1_5	map_l250_m2_e1	*	56.3873	42.7027	82.9787	91.9105	79	106	78	16	14	87.5000
mlin-fermikit	INDEL	I1_5	map_siren	hetalt	82.7225	70.5357	100.0000	83.1169	79	33	78	0	0
mlin-fermikit	INDEL	I6_15	map_l100_m2_e0	*	76.7503	68.1034	87.9121	83.6036	79	37	80	11	10	90.9091
mlin-fermikit	INDEL	I6_15	map_l100_m2_e1	*	76.7503	68.1034	87.9121	83.9789	79	37	80	11	10	90.9091
mlin-fermikit	SNP	*	tech_badpromoters	homalt	95.1807	98.7500	91.8605	44.8718	79	1	79	7	6	85.7143
mlin-fermikit	SNP	ti	tech_badpromoters	*	94.0476	92.9412	95.1807	40.7143	79	6	79	4	4	100.0000
mlin-fermikit	SNP	tv	map_l250_m0_e0	homalt	47.1642	40.9326	55.6338	80.3051	79	114	79	63	60	95.2381
qzeng-custom	INDEL	D16_PLUS	map_l100_m2_e1	*	36.6856	81.4433	23.6749	89.0986	79	18	67	216	1	0.4630
rpoplin-dv42	INDEL	I6_15	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged	hetalt	96.3415	92.9412	100.0000	56.2842	79	6	80	0	0
rpoplin-dv42	SNP	*	tech_badpromoters	homalt	98.7500	98.7500	98.7500	50.9202	79	1	79	1	1	100.0000
raldana-dualsentieon	INDEL	D6_15	map_l150_m2_e0	*	98.1366	96.3415	100.0000	89.8718	79	3	79	0	0
raldana-dualsentieon	INDEL	I6_15	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged	hetalt	96.3415	92.9412	100.0000	56.0440	79	6	80	0	0
raldana-dualsentieon	SNP	*	tech_badpromoters	homalt	98.1366	98.7500	97.5309	46.0000	79	1	79	2	2	100.0000
raldana-dualsentieon	SNP	*	map_siren	hetalt	97.5000	96.2963	98.7342	67.0833	78	3	78	1	1	100.0000
raldana-dualsentieon	SNP	tv	map_siren	hetalt	97.5000	96.2963	98.7342	67.0833	78	3	78	1	1	100.0000
rpoplin-dv42	INDEL	D1_5	map_siren	hetalt	95.7055	92.8571	98.7342	91.2804	78	6	78	1	1	100.0000
raldana-dualsentieon	INDEL	D16_PLUS	map_l100_m1_e0	*	88.6364	89.6552	87.6404	92.1793	78	9	78	11	4	36.3636
raldana-dualsentieon	INDEL	D1_5	map_siren	hetalt	96.2963	92.8571	100.0000	89.3151	78	6	78	0	0
jli-custom	INDEL	D16_PLUS	map_l100_m1_e0	*	91.2281	89.6552	92.8571	92.4866	78	9	78	6	2	33.3333
jli-custom	INDEL	I16_PLUS	map_siren	*	94.5527	90.6977	98.7500	90.1840	78	8	79	1	0	0.0000
jli-custom	INDEL	I1_5	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged	homalt	92.4901	95.1220	90.0000	74.9304	78	4	81	9	9	100.0000
ltrigg-rtg1	INDEL	D1_5	map_siren	hetalt	95.1069	92.8571	97.4684	93.1245	78	6	77	2	2	100.0000
ltrigg-rtg1	INDEL	I16_PLUS	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged	het	83.8710	72.2222	100.0000	64.4231	78	30	74	0	0
ltrigg-rtg1	INDEL	I1_5	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged	hetalt	96.2963	92.8571	100.0000	67.2000	78	6	82	0	0
gduggal-bwafb	INDEL	D6_15	map_l150_m2_e1	*	94.6014	91.7647	97.6190	90.6977	78	7	82	2	1	50.0000
gduggal-bwafb	INDEL	*	map_l100_m2_e1	hetalt	73.5849	59.0909	97.5000	93.2660	78	54	39	1	1	100.0000
gduggal-bwaplat	INDEL	D1_5	func_cds	het	95.7055	91.7647	100.0000	60.4061	78	7	78	0	0
eyeh-varpipe	INDEL	I6_15	map_l100_m1_e0	*	76.4706	68.4211	86.6667	74.6424	78	36	169	26	24	92.3077
asubramanian-gatk	INDEL	D16_PLUS	map_l100_m2_e0	*	87.1508	86.6667	87.6404	95.9118	78	12	78	11	3	27.2727
bgallagher-sentieon	INDEL	I16_PLUS	lowcmp_AllRepeats_51to200bp_gt95identity_merged	hetalt	95.1220	90.6977	100.0000	77.4869	78	8	86	0	0
bgallagher-sentieon	INDEL	I1_5	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged	homalt	88.6364	95.1220	82.9787	75.7106	78	4	78	16	16	100.0000
bgallagher-sentieon	INDEL	I6_15	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged	het	98.1132	96.2963	100.0000	78.9189	78	3	78	0	0
bgallagher-sentieon	SNP	*	map_siren	hetalt	98.1132	96.2963	100.0000	69.5312	78	3	78	0	0
bgallagher-sentieon	SNP	tv	map_siren	hetalt	98.1132	96.2963	100.0000	69.5312	78	3	78	0	0
astatham-gatk	INDEL	I16_PLUS	lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged	*	93.4132	89.6552	97.5000	85.0187	78	9	78	2	2	100.0000

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