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e term haplotype refers to ‘
A. DNA Polymorph
 
      
  
  
first complete ger
  
 
 
 
+3. Sanger sequenced thi i a
1-4, Minisatellites, also known as n which the repeat unit is up to bpin
length
+ 5. Microsatellites, also called .. +, whose repeats are usually bpor
      
 
   
 
 
  
  
 
  
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ea
13. Genome scaffolding
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ne evaluates three vital accuracy
 
 
  
ly is divided into two basie areas.
 
 
ing at the same position in genomic DNA trom different
    
 
lecular markers such as...
   
(92215) ib 15 oe nl Ansell Saga 2 38
1, What does the typical NGS workflow consist of?
 
  
  
    
 
 
adaptor ligation, and data
ings li \d PCR
tion, and PCR
 
    
2. How does
ay By coi
b. By compa
By looking 9
d. By breaking down
 
the results of pyroyequenc
of nucteotides present in the DNA.
zyme tags associated with
correspond with
ng the byproducts,
 
 
 
h nucleotide.
1g. nucleotide,
   
    
a dd
 
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€ Unique DNA sequence
 f, Long repetitive regions of DNA sequ
g. Multiple 1¢ reads on both str
bh. igh-q
s causes difficulties
 
assembling a contig?
    
nds,
  
 
ity sequence reads.
sie stith the following genes: AaBb x aabb. They had 400 offspriv
Of these, there were 150 AaBb, 50 Aabb, b and 150 aabb. Are these genes linked? II s
calculate the MU. Gans
A. Yes; 33 MU
 
 
B. Yes: 25 MU
C. Ampossible to determine
D. No
S.A type of whole genome sequencing called Sanger Sequencing was used (0 Sequence the first
human genome. at ‘
 
    
 
rue B. False
6. coverage depth results in increased confidence in variant identification.
A. Decreased 7 —Beincreased C. Equal
7. Whole genome sequencing methods include:
‘A. Clone-by-clone _B Whole genome shotgun
C. Both A and B Neither
 
8. Genetic markers are portions of a ‘whose inheritance patterns can be followed,
A. unidentifiable, genes
B. unidentifiable, chromosome i
_-G. identifiable, chromosome
D. identifiable, genes *
72 Strenaihs of whole genome sequencing using next-generation sequencing methods include:
‘A. Ability to obtain information on the entire genome
B. Less costly than traditional n
C. Faster time compared to tra
D. All of the above
10. In automated DNA sequencing _
'A, Radio-labelled dNTPs are used
B.  Radio-labelled ddNTPs are used
77 © Fluorescently labelled dNTPs are used
D, Fluorescently labelled dNTPs are used
1h of the following is untrue about the genome mapping?
It doesn’t lead (0 the understanding of a genome structure
It involves identifying the relative locations of genes
 
 
 
inheritance patterns.
A. remotely related (0
B. related
C. regardless of
1D. assoctated with
‘can comprise a large proportion of the eukaryotic genome a!
ransposable elements, single cops sequences
{transposable elements, repetitive sequences
macrosatellite DNA elements, single copy sequences
satellite DNA elements, single copy sequencesSpall acl aS pupaally all Sang |
14. variation in the length ofa restriction fragment detected by @ particular probe due (o
hneleotide changes a a restriction site
A. AFLP B.SSLP ZO RELP D. RAPD
 
 
 
   
 
 
15. In medical applications, the ultimate goal of gene mapping isto disease zene.
: A. True False
16, The genome annotation process involves two steps: gene predi
| LX True B, False
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1. Gene structures a
2. Prokaryotic genomes con
genes. K
  
 
include introns in protein-coding
3. The pairwise alignment programs are wot inyolved in gene annotation processes 7
‘ 4. Biological processes are not described in gene ontology (GO)
5. Ifa newly sequenced gene or its gene product has signifi
of functional assignment is taking place —
6. The centromeric and telomeric regions are located
 
   
matches with a dat
 
ase sequence, 3
transfe
 
 
 
  
    
    
 
 
 
 
       
    
      
+ in linkage mapping correlate with a specifi rs ee
s frequencies between two liked genes are never eS
9. Upstream regutatory sequences can be used to locate the regions where genes bes
10. A sequence-tagged site (STS) is unique and easily recognizable ——
11. OLC starts withthe fragmentation process fr each read inset of reads (R) into
length called Kemers
. 12, Genes that arose by duplication within a species called ortholog + ~
1B. Prendagedie isa nonf faonily ge—
14, expressed sequence tags ean be considered STS markers.
18, The number of repetitive elements fiideal (ond
: 16, Protei ified by searching for open reading fr:
 
 
(215) fi D Ali Cgc) ge HES Ce al ASNT AL Ce ah
A. Bfiefly Mention the main classification of eukaryotic genome structure
i B. You are working as part of a research team studying the structure and function of a particular
‘gene. What specific techniques or approaches would you use?
Describe how the DNA sequence is obtained by (A) pyrosequencing, (8) Nanopore
The figure depicted below showcases a substantial reduction in the cost associated with
sequencing the human genome. Provide a brief discussion on this trend
 
 
9
  
  
Source (https://www.genome.gov/about-genomics/fact-sheets/DNA-Sequencing-Costs-Data}
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Discuss Therapeutic protein as novel Strategy for chronic genetic diseases using
Biotechnology Tools.
2 ESS Se Ee
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Explain the role of different types of stem cells therapy in cloning, compare
with the parallel somatic cell nuclear transfer (SCNT).
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Ql: define the following:
1- BLUETOOTH PROTOCOL STACK
2- ETHERNET.
3-1Pv4 and IPV6
4- CLASSIFICATION OF BLUETOOTH
5. THE DIFFERENT BLUETOOTH GENERATION
(02: explain the differences between (repeate!s, barrel eonnectors. hubs. switches. LOuers
 
and bridges)? oe 10 marks)
13: compare the following: (10 marks)
AICP and IP protocols
2-CAT Seand CATS
Q4: complete the following: (10 marks)
L-IMAP referred to.. but SNMP referred to.
   
. moreover ICMP referred to...
but MAN topology used to.
moreover Master CLIENT
 
OSI referred to...
 
 
3-WAN network topology used to.
  
4- Slave CLIENT referred (0...
referred to..
5 PUNCHING TOOL used for ...
in network infrastructure.
networks.
 
    
. but in PATCH PANEL used for
 
   
.-and in Cat.6
 
 
 
. but UDP protocol referred
 
7-TFTP protocol referred (0 soseecessee
Cee ~
g-In COAXIAL CABLE the connector used is.....
PAIR used =
9-The ma
10-'The FACEPLATES used f07 ....cssuseeeo But DATA ENCAPSUL:
- in LAN network connections. oe
 
but TWISTED
 
 
ut in CAT.3 is
 
 
 
meansSt explain the different types of Bluetooth applications in data communications using
Smart electronic devices: (0 marks)
Q6: choose the correct answer, (10 marks)
1) which layer does th
frames for transmissio
 
 
data link layer taxe packets from and encapsulate them into
 
a) transport layer b) application layer _¢) network layer d) physical layer
2 which of the followin,
    
is not a network edge dev
a)switch by PC ©) smartphores 4d) servers
3) what is the term for the data commu
 
ication system within a building or campus:
a)MAN  b)LAN — e) WAN) none of the above
4) which layer provides and supports points-to-point as well as broadcast
‘communication
 
 
a)network layer —b)datalink layer _¢) session layer _d) application layer
5) SMTP protocol response for:
a) emails communications b) multimedia communications |
© small data 4) none of the above
The questions are over.
Dest Wishes son
Dr. / Tarek Wrshana
Dr. / E-hosiny Bosila2.
 
 
  
 
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Complete the follwing sentences with the correct answers
Create a numeric vector and store the vector as a variable with this value 4.6,
53000, 50000
a variable called species .
variable called combined ......
List all of the files in /bin that cor
in /bin that end with the
  
then construct another vector cont h and ecoli in
   
. And assign the two previous vectors ina ney
  
   
then List all of the files
   
etter ‘0
 
rash, we use the
To change the directory.
 
Po cheek the present working directory i
is used to make a new directory and
     
 
 
Createa M: 12 of 4 columns and 5 rows
samples genes .
Suppose we want to see how many reads are in our file Mov10_oe_I.subset.fq contain “bad”
data reads with 10 consecutive Ns (NNNNNNNNNN) what the com
then rename the
 
 
And rows
     
 
 
  
Create a vector named sample-group with
out KO") values, and 3 over-expre
factor data structure.
use the commands we
many unique exons
e elements: 3 control (*CTL’
OB”) values, and turn the sample.
  
 
  
   
 
bout our data: how
wes. gtt file’
 
simple questi
19
  
         
re present on chromosome 1 using ehrt-l
43920)
 
 
Create a seript that would do the following each time we get a new data set
nFASTQ file
2 ou
cds into a new file
+ Use for loop to
 
(erate over
 
+ Generate a prefix to use for nat
+ Dumprolt bad r
+ Geta count of the number of bad reads and report it to a running log.
 
{put files
 
 
BY cst
GAs Clty LL hl