Menu
Research Publication

Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery.

Ghorbani Mohammadmersad, M Moosa, Shabir S et al.

40325133 PubMed ID
100 Authors
2025-05-05 Published
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GM
Ghorbani Mohammadmersad
MM
M Moosa
SS
Shabir S
SZ
Siddig Zenab
ZF
Z Farhad
RR
Radi R
NH
Naeem Haroon
HH
H Harvey
WT
William T WT
MF
Mastrorosa Francesco Kumara
FM
FK Munson
KM
Katherine M KM
MR
Mohamad Razali Rozaimi
RA
R Aliyev
EE
Elbay E
DI
Diboun Ilhame
IA
I Abouelhassan
RR
Rawan R
TM
Tauro Melissa
MH
M Hassan
SS
Sondoss S
MR
Mathew Rebecca
RA
R Al Hashmi
MM
Muna M
ML
Mathew Lisa S
LW
LS Wang
KK
Kun K
SA
Salhab Abdul Rahman
AV
AR Vempalli
FR
Fazulur Rehaman FR
EK
El Khouly Ahmed
AA
A Alazwani
II
Iman I
TS
Tomei Sara
SF
S Fakhro
KA
Khalid A KA
SA
Satti Alia
AB
A Benini
RR
Ruba R
RA
Rhie Arang
AE
A Eichler
EE
Evan E EE
MY
Mokrab Younes
YI
Y Ismail
SI
Said I SI
AW
Al-Muftah Wadha
WB
W Badji
RR
Radja R
MH
Mbarek Hamdi
HD
H Darwish
DD
Dima D
FT
Fadl Tasnim
TY
T Yasin
HH
Heba H
EM
Ennaifar Maryem
MA
M Abdellatif
RR
Rania R
AF
Alkuwari Fatima
FA
F Alvi
MM
Muhammad M
AY
Al-Sarraj Yasser
YS
Y Saad
CC
Chadi C
AA
Althani Asmaa
AF
A Fethnou
EE
Eleni E
QF
Qafoud Fatima
FA
F Alkhayat
EE
Eiman E
AN
Afifi Nahla
NL
N Liu
WW
Wei W
LS
Lorenz Stephan
SS
S Syed
NN
Najeeb N
AH
Almabrazi Hakeem
HT
H Temanni
RR
Ramzi R
ST
Saqri Tariq Abu
TK
TA Khatib
MM
Mohammedhusen M
HM
Hamza Mehshad
MZ
M Zaid
TA
Tariq Abu TA
PT
Pathare Tushar
TP
T Poolat
SS
Shafeeq S
AR
Al-Ali Rashid
RA
R Albagha
OO
Omar O
AS
Al-Khodor Souhaila
SA
S Alshafai
MM
Mashael M
BR
Badii Ramin
RC
R Chouchane
LL
Lotfi L
EX
Estivill Xavier
XF
X Fakhro
KK
Khalid K
PJ
Puthen Jithesh V
Chapter II

Abstract

Summary of the research findings

Advances in long-read sequencing have enabled routine complete assembly of human genomes, but much remains to be done to represent broader populations and show impact on disease-gene discovery. Here, we report highly accurate, near-complete and phased genomes from six Middle Eastern (ME) family trios (n = 18) with neurodevelopmental conditions, representing ancestries from Sudan, Jordan, Syria, Qatar and Afghanistan. These genomes revealed 42.2 Mb of new sequence (13.8% impacting known genes), 75 new HLA/KIR alleles and strong signals of inbreeding, with ROH covering up to one-third of chromosomes 6 and 12 in one individual. Using assembly-based variant calling, we identified 23 de novo and recessive variants as strong candidates for causing previously unresolved symptoms in the probands. The ME genomes revealed unique variation relative to existing references, showing enhanced mappability and variant calling. These results underscore the value of de novo assembly for disease variant discovery and the need for sampled ME-specific references to better characterize population-relevant variation.

Chapter III

Analysis

Comprehensive review of ancestry and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Summary

Key Findings

Ancestry Insights

Traits Analysis

Historical Context

Scientific Assessment