statistiche ricercatore

Nazione	#
US - Stati Uniti d'America	1.069
SG - Singapore	167
GB - Regno Unito	138
CN - Cina	133
IT - Italia	89
DE - Germania	77
HK - Hong Kong	73
IN - India	56
CA - Canada	46
KR - Corea	46
VN - Vietnam	45
RU - Federazione Russa	41
SE - Svezia	36
AU - Australia	26
CI - Costa d'Avorio	25
TG - Togo	25
FR - Francia	24
BR - Brasile	23
IE - Irlanda	23
JP - Giappone	23
TR - Turchia	21
ZA - Sudafrica	21
ES - Italia	18
TW - Taiwan	18
NL - Olanda	15
SC - Seychelles	14
IL - Israele	13
EE - Estonia	10
PK - Pakistan	8
CH - Svizzera	7
FI - Finlandia	7
IR - Iran	7
BE - Belgio	6
UA - Ucraina	6
AR - Argentina	5
PH - Filippine	5
AT - Austria	4
IQ - Iraq	4
NO - Norvegia	4
TH - Thailandia	4
CY - Cipro	3
DZ - Algeria	3
ET - Etiopia	3
HR - Croazia	3
MO - Macao, regione amministrativa speciale della Cina	3
MY - Malesia	3
PT - Portogallo	3
RO - Romania	3
SA - Arabia Saudita	3
CD - Congo	2
DK - Danimarca	2
EC - Ecuador	2
EG - Egitto	2
ID - Indonesia	2
LB - Libano	2
MX - Messico	2
PL - Polonia	2
SI - Slovenia	2
UG - Uganda	2
BD - Bangladesh	1
CL - Cile	1
CO - Colombia	1
KH - Cambogia	1
LT - Lituania	1
NA - Namibia	1
NZ - Nuova Zelanda	1
PE - Perù	1
QA - Qatar	1
SY - Repubblica araba siriana	1
VE - Venezuela	1
Totale	2.440

Nome	#
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods	1.028
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges	203
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI	153
Bioinformatics for personal genome interpretation	144
Collective judgment predicts disease-associated single nucleotide variants	138
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges	136
SNP-SIG 2013: The state of the art of genomic variant interpretation	122
SNP-SIG 2013: From coding to non-coding - New approaches for genomic variant interpretation	113
SNP-SIG Meeting 2011: identification and annotation of SNPs in the context of structure, function, and disease	94
null	67
null	63
VarI-SIG 2015: Methods for personalized medicine - the role of variant interpretation in research and diagnostics	62
null	60
VarI-SIG 2014--From SNPs to variants: interpreting different types of genetic variants	57
Thoughts from SNP-SIG 2012: future challenges in the annotation of genetic variations	55
Totale	2.495

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	96	0	0	0	0	0	10	0	8	18	11	7	42
2021/2022	149	14	2	4	4	29	13	2	13	13	1	13	41
2022/2023	199	16	41	11	14	11	17	3	14	29	17	10	16
2023/2024	742	0	10	5	8	3	6	0	16	126	244	179	145
2024/2025	480	118	92	23	18	64	30	19	18	10	12	22	54
2025/2026	331	69	60	67	45	64	26	0	0	0	0	0	0
Totale													2.495

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